61. World Of Ophthalmology - Orbital Implants OTHER LINKS (18). List of the Sites' Home Pages. American Society of OphthalmicPlastic Reconstructive Surgery (ASOPRS) anophthalmos And Orbital Implants, _. http://wmed.narod.ru/w_ophth/surgery/s_32.htm

W orld of Medicine - Ophthalmology Ophthalmology - Home Page Anatomy Physiology Diseases ... Diagnostic Tests Surgical Procedures Medications Journals Images Links ... Index (A-Z) Encyclopaedia of Ophthalmology - Greatest Links' Collection Ophthalmologic Surgical Procedures Oculoplastic Surgical Procedures Orbital Implants ORBITAL IMPLANTS MeSH description Rounded objects made of coral, teflon, or alloplastic polymer and covered with sclera, and which are implanted in the orbit following enucleation. An artificial eye is usually attached to the anterior of the orbital implant for cosmetic purposes. SEARCH ENGINES AltaVista Yahoo Lycos Dogpile Search for Orbital Implants Medical Matrix eMedicine Search for Orbital Implants ARTICLES, NEWS, CONFERENCES HON CliniWeb Ophtholinx Ophthalmic Journals OnLine Search Articles for Orbital Implants OTHER LINKS List of the Sites' Home Pages Anophthalmos And Orbital Implants Dr. Steven C. Dresner's Web Site: Primary Orbital Implant Placement with Evisceration Articles Eye Cancer Network: Orbital Implants (Volume-Replacement After Enucleation) EyeMDLink: Orbital Reconstruction / Ocular Prosthetics (False Eyes) Patients Information EyePlastics.com - Dr. Mark Brown's Site:

62. Linkage.rockefeller.edu/wli/omim/auto_rec.txt ANIRIDIA, CEREBELLAR ATAXIA, AND MENTAL DEFICIENCY *206780 ANODONTIA, COMPLETE,OF PERMANENT DENTITION *206800 ANONYCHIA *206900 anophthalmos, TRUE OR http://linkage.rockefeller.edu/wli/omim/auto_rec.txt

*200150 : CHOREOACANTHOCYTOSIS; CHAC *200350 : ACETYL-CoA CARBOXYLASE DEFICIENCY *200400 : ACHALASIA, FAMILIAL ESOPHAGEAL *200500 : ACHEIROPODY *200600 : ACHONDROGENESIS, TYPE IA; ACG1A *200990 : ACROCALLOSAL SYNDROME; ACLS *201000 : ACROCEPHALOPOLYSYNDACTYLY TYPE II *201100 : ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE; AEZ *201300 : ACROOSTEOLYSIS, NEUROGENIC *201400 : ACTH DEFICIENCY *201450 : ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN; ACADM *201460 : ACYL-CoA DEHYDROGENASE, LONG-CHAIN, DEFICIENCY OF *201470 : ACYL-CoA DEHYDROGENASE, SHORT-CHAIN; ACADS *201475 : ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF *201550 : ADDUCTED THUMBS SYNDROME *201810 : ADRENAL HYPERPLASIA II *201910 : ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY *202010 : ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 11-@BETA-HYDROXYLASE DEFICIENCY *202110 : ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY *202200 : ADRENAL UNRESPONSIVENESS TO ACTH *202500 : SEVERE COMBINED IMMUNODEFICIENCY 1; SCID1 *203100 : ALBINISM I *203200 : ALBINISM II *203300 : HERMANSKY-PUDLAK SYNDROME; HPS *203500 : ALKAPTONURIA *203650 : ALOPECIA-MENTAL RETARDATION SYNDROME *203700 : ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC CIRRHOSIS *203740 : ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY *203750 : ALPHA-METHYLACETOACETICACIDURIA *203800 : ALSTROM SYNDROME; ALMS1 *204200 : CEROID LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3 *204300 : CEROID LIPOFUSCINOSIS, NEURONAL 4; CLN4 *204400 : AMAUROTIC IDIOCY, CONGENITAL FORM *204500 : CEROID LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2 *204600 : AMAUROTIC IDIOCY, LATE INFANTILE TYPE, WITH MULTILAMELLAR CYTOSOMES *204700 : AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE *204800 : AMOBARBITAL, DEFICIENT N-HYDROXYLATION OF *205100 : AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2 *205200 : AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA *206500 : ANENCEPHALY *206570 : ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT *206700 : ANIRIDIA, CEREBELLAR ATAXIA, AND MENTAL DEFICIENCY *206780 : ANODONTIA, COMPLETE, OF PERMANENT DENTITION *206800 : ANONYCHIA *206900 : ANOPHTHALMOS, TRUE OR PRIMARY *206920 : ANOPHTHALMOS WITH LIMB ANOMALIES *207410 : ANTLEY-BIXLER SYNDROME; ABS *207750 : APOLIPOPROTEIN C-II DEFICIENCY, TYPE I HYPERLIPOPROTEINEMIA DUE TO *207800 : ARGININEMIA *207900 : ARGININOSUCCINICACIDURIA *208000 : ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY *208060 : ARTERIOSCLEROSIS, SEVERE JUVENILE *208100 : ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN *208150 : PENA-SHOKEIR SYNDROME, TYPE I *208200 : ARTHROGRYPOSIS-LIKE DISORDER *208230 : ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD; PPAC *208250 : ARTHROPATHY-CAMPTODACTYLY SYNDROME *208400 : ASPARTYLGLUCOSAMINURIA *208500 : ASPHYXIATING THORACIC DYSTROPHY; ATD *208750 : ATAXIA, DEAFNESS, AND CARDIOMYOPATHY *208800 : PYRUVATE DECARBOXYLASE DEFICIENCY *208900 : ATAXIA-TELANGIECTASIA; AT *208905 : ATAXIA-TELANGIECTASIA, COMPLEMENTATION GROUP D; ATD; ATDC *209100 : ATONIC-ASTATIC SYNDROME OF FOERSTER *209900 : BARDET-BIEDL SYNDROME, TYPE 2; BBS2 *209901 : BARDET-BIEDL SYNDROME, TYPE 1; BBS1 *210100 : BETA-AMINOISOBUTYRIC ACID, URINARY EXCRETION OF *210200 : BETA-METHYLCROTONYLGLYCINURIA I *210250 : SITOSTEROLEMIA *210370 : BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY *210600 : BIRD-HEADED DWARFISM *210710 : MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I *210720 : MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II *210730 : MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III *210900 : BLOOM SYNDROME; BLM *211100 : FUCOSYLTRANSFERASE 1; FUT1 *211180 : BOWEN HUTTERITE SYNDROME *211350 : BOWING, CONGENITAL, WITH SHORT BONES *211390 : BRITTLE HAIR AND MENTAL DEFICIT *211410 : BREAST CANCER, DUCTAL, 1; BRCD1 *211420 : BREAST CANCER, DUCTAL, 2; BRCD2 *211500 : BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD *211530 : BULBAR PALSY, PROGRESSIVE, WITH PERCEPTIVE DEAFNESS *211750 : C SYNDROME *211890 : CAMPOMELIA, CUMMING TYPE *211900 : CALCINOSIS, TUMORAL, WITH HYPERPHOSPHATEMIA *211960 : CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMAL PALMAR CREASES *212050 : CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS; FCMC *212130 : CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH *212138 : CARNITINE-ACYLCARNITINE TRANSLOCASE; CACT *212160 : CARNITINE DEFICIENCY, MYOPATHIC *212200 : CARNOSINEMIA *212350 : CATARACT AND CARDIOMYOPATHY *212400 : CATARACT AND CONGENITAL ICHTHYOSIS *212500 : CATARACT, CONGENITAL OR JUVENILE *212780 : CENANI SYNDACTYLISM *212840 : CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM *212895 : CEREBELLAR ATAXIA, EARLY-ONSET, WITH RETAINED TENDON REFLEXES; EOCA *213000 : CEREBELLAR HYPOPLASIA *213100 : CEREBELLOPARENCHYMAL DISORDER II; CPD II *213200 : CEREBELLAR ATAXIA 1; CLA1 *213300 : CEREBELLOPARENCHYMAL DISORDER IV; CPD IV *213600 : CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC *213700 : CEREBROTENDINOUS XANTHOMATOSIS *213980 : CEREBROFACIOTHORACIC DYSPLASIA *214110 : CEREBROHEPATORENAL SYNDROME, VARIANT TYPES *214370 : NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION, AND ABSENT SENSORY LARGE MYELINATED FIBERS *214400 : CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A *214500 : CHEDIAK-HIGASHI SYNDROME; CHS1 *214900 : CHOLESTASIS-LYMPHEDEMA SYNDROME *214950 : CHOLESTASIS, INTRAHEPATIC, WITH DEFECTIVE METABOLISM OF TRIHYDROXYCOPROSTANIC ACID TO CHOLIC ACID *215400 : CHORDOMA *215470 : CHORIORETINAL DYSTROPHY, SPINOCEREBELLAR ATAXIA, AND HYPOGONADOTROPIC HYPOGONADISM *215500 : CHOROIDAL DYSTROPHY, CENTRAL AREOLAR; CACD *215520 : CILIARY DYSKINESIA DUE TO TRANSPOSITION OF CILIARY MICROTUBULES *216340 : CLEIDOCRANIAL DYSPLASIA WITH MICROGNATHIA, ABSENT THUMBS, AND DISTAL APHALANGIA *216400 : COCKAYNE SYNDROME, TYPE I; CKN1 *216550 : COHEN SYNDROME; COH1 *216700 : COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING; RPC *216950 : COMPLEMENT COMPONENT C1r DEFICIENCY *217000 : COMPLEMENT COMPONENT 2 DEFICIENCY *217030 : I FACTOR; IF *217050 : COMPLEMENT COMPONENT 6 DEFICIENCY *217070 : COMPLEMENT COMPONENT 7 DEFICIENCY *217300 : CORNEA PLANA 2; CNA2 *217400 : CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS *217500 : CORNEAL DYSTROPHY, BAND-SHAPED *217700 : CORNEAL ENDOTHELIAL DYSTROPHY 2; CHED2 *217800 : MACULAR DYSTROPHY, CORNEAL, 1; MCDC1 *218000 : CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY *218030 : CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY *218040 : COSTELLO SYNDROME *218100 : CRANIAL NERVES, CONGENITAL PARESIS OF *218330 : CRANIOECTODERMAL DYSPLASIA *218400 : CRANIOMETAPHYSEAL DYSPLASIA, RECESSIVE TYPE *218900 : CROME SYNDROME *219000 : CRYPTOPHTHALMOS WITH OTHER MALFORMATIONS *219100 : CUTIS LAXA *219150 : CUTIS LAXA, CORNEAL CLOUDING, AND MENTAL RETARDATION *219500 : CYSTATHIONINURIA *219800 : CYSTINOSIS, NEPHROPATHIC; CTNS *220111 : LEIGH SYNDROME, FRENCH-CANADIAN TYPE *220120 : D-GLYCERICACIDEMIA *220150 : DALMATIAN HYPOURICEMIA *220210 : DANDY-WALKER-LIKE MALFORMATION WITH ATRIOVENTRICULAR SEPTAL DEFECT *220500 : DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, RECESSIVE FORM *221300 : DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR *221350 : DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA *221650 : DEAFNESS, NEURAL, PROGRESSIVE CHILDHOOD TYPE *221770 : POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL *221800 : DERMOCHONDROCORNEAL DYSTROPHY *221900 : DETACHMENT OF RETINA, CONGENITAL *222100 : DIABETES MELLITUS, INSULIN-DEPENDENT, 1; IDDM1 *222300 : WOLFRAM SYNDROME *222600 : DIASTROPHIC DYSPLASIA; DTD *222690 : DIBASICAMINOACIDURIA I *222745 : 2,4-@DIENOYL-CoA REDUCTASE; DECR *222748 : DIHYDROPYRIMIDINASE; DPYS *222800 : DIPHOSPHOGLYCERATE MUTASE DEFICIENCY OF ERYTHROCYTE *222900 : DISACCHARIDE INTOLERANCE I *223000 : LACTASE DEFICIENCY, CONGENITAL *223100 : DISACCHARIDE INTOLERANCE III *223360 : DOPAMINE BETA-HYDROXYLASE, PLASMA; DBH *223370 : DUBOWITZ SYNDROME *223800 : DYGGVE-MELCHIOR-CLAUSEN DISEASE *223900 : DYSAUTONOMIA, FAMILIAL; DYS *224050 : DYSEQUILIBRIUM SYNDROME; DES *224100 : ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II; CDAN2 *224120 : ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE I; CDAN1 *224300 : DYSOSTEOSCLEROSIS *224500 : DYSTONIA MUSCULORUM DEFORMANS 2; DYT2 *224690 : EAR, PATELLA, SHORT STATURE SYNDROME *224750 : SCHOPF-SCHULZ-PASSARGE SYNDROME *225000 : ECTODERMAL DYSPLASIA, CLEFT LIP AND PALATE, HAND AND FOOT DEFORMITY, AND MENTAL RETARDATION *225060 : ECTODERMAL DYSPLASIA, TYPE 4; ED4 *225200 : ECTOPIA LENTIS WITH ECTOPIA OF PUPIL *225250 : ECTOPIC THYROID WITH HYPOTHYROIDISM *225280 : EEM SYNDROME *225410 : EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE *225500 : ELLIS-VAN CREVELD SYNDROME; EVC *225750 : ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH CALCIFICATION OF BASAL GANGLIA AND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS *225790 : ENCEPHALOCLASTIC PROLIFERATIVE VASCULOPATHY; EPV *226200 : ENTEROKINASE DEFICIENCY *226300 : ENTEROPATHY, PROTEIN-LOSING *226450 : EPIDERMOLYSIS BULLOSA INVERSA DYSTROPHICA *226500 : EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA *226750 : EPILEPSY AND YELLOW TEETH *226900 : EPIPHYSEAL DYSPLASIA, MULTIPLE *226960 : EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS *226980 : EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS *227090 : ERYTHRODERMA, LETHAL CONGENITAL *227150 : ETHANOLAMINOSIS *227220 : EYE COLOR 3; EYCL3 *227240 : EYE COLOR 1; EYCL1 *227260 : FACIAL ECTODERMAL DYSPLASIA *227330 : FACIODIGITOGENITAL SYNDROME, RECESSIVE *227400 : FACTOR V DEFICIENCY *227500 : FACTOR VII DEFICIENCY *227600 : FACTOR X DEFICIENCY *227645 : FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC *227646 : FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD *227650 : FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA *227660 : FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB *228000 : FARBER LIPOGRANULOMATOSIS *228100 : FATTY METAMORPHOSIS OF VISCERA *228250 : FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY *228520 : FIBROCHONDROGENESIS *228600 : FIBROMATOSIS, JUVENILE HYALINE *228900 : FIBULA APLASIA AND COMPLEX BRACHYDACTYLY *228960 : FLAUJEAC FACTOR DEFICIENCY *229000 : FLETCHER FACTOR DEFICIENCY *229050 : FOLIC ACID, TRANSPORT DEFECT INVOLVING *229100 : FORMIMINOTRANSFERASE DEFICIENCY *229200 : FRAGILITAS OCULI WITH JOINT HYPEREXTENSIBILITY *229300 : FRIEDREICH ATAXIA 1; FRDA *229400 : FRONTOFACIONASAL DYSOSTOSIS *229500 : FRUCTOSE AND GALACTOSE INTOLERANCE *229600 : FRUCTOSE INTOLERANCE, HEREDITARY *229700 : FRUCTOSE-1,6-BISPHOPHATASE 1; FBP1 *229800 : FRUCTOSURIA *229850 : FRYNS SYNDROME; FRNS *230000 : FUCOSIDOSIS *230200 : GALACTOKINASE DEFICIENCY *230350 : GALACTOSE EPIMERASE DEFICIENCY *230400 : GALACTOSEMIA *230450 : GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO *230500 : GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I *230700 : GANGLIOSIDOSIS, GM2, TYPE III, OR JUVENILE TYPE *230740 : GAPO SYNDROME *230800 : GAUCHER DISEASE, TYPE I *231050 : GELEOPHYSIC DYSPLASIA *231070 : GERODERMA OSTEODYSPLASTICA; GO *231090 : HYDATIDIFORM MOLE *231200 : GIANT PLATELET SYNDROME *231500 : GLAUCOMA, JUVENILE *231550 : ACHALASIA-ADDISONIANISM-ALACRIMIA SYNDROME; AAA *231610 : GLUCURONIDASE, MOUSE, MODIFIER OF; GUSM *231670 : GLUTARICACIDEMIA I *231675 : GLUTARICACIDURIA IIC *231680 : GLUTARICACIDURIA IIA *231950 : GLUTATHIONURIA *232000 : PROPIONICACIDEMIA, TYPE I *232050 : PROPIONICACIDEMIA, TYPE II *232200 : GLYCOGEN STORAGE DISEASE I *232300 : GLYCOGEN STORAGE DISEASE II *232400 : GLYCOGEN STORAGE DISEASE III *232500 : GLYCOGEN STORAGE DISEASE IV *232600 : GLYCOGEN STORAGE DISEASE V *232700 : GLYCOGEN STORAGE DISEASE VI *232800 : GLYCOGEN STORAGE DISEASE VII *233100 : RENAL GLUCOSURIA; GLYS1 *233400 : GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS *233690 : GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-NEGATIVE FORM *233700 : GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-POSITIVE FORM I *233710 : GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-POSITIVE FORM II *234000 : HAGEMAN FACTOR DEFICIENCY *234050 : HAIR-BRAIN SYNDROME *234200 : HALLERVORDEN-SPATZ DISEASE *234500 : HARTNUP DISORDER *235200 : HEMOCHROMATOSIS; HFE *235510 : HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME *235800 : HISTIDINEMIA *235830 : HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT *235900 : HISTIOCYTOSIS, FAMILIAL LIPOCHROME *236100 : HOLOPROSENCEPHALY 1, ALOBAR; HPE1 *236200 : HOMOCYSTINURIA *236250 : 5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR *236400 : HUMERORADIAL SYNOSTOSIS *236670 : WALKER-WARBURG SYNDROME *236680 : HYDROLETHALUS SYNDROME *236700 : MCKUSICK-KAUFMAN SYNDROME; MKKS *236730 : UROFACIAL SYNDROME; UFS *236792 : L-2-@HYDROXYGLUTARICACIDEMIA *236795 : 3-@HYDROXYISOBUTYRICACIDURIA *236800 : HYDROXYKYNURENINURIA *236900 : HYDROXYLYSINURIA *237000 : HYDROXYPROLINEMIA *237300 : HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY *237310 : HYPERAMMONEMIA DUE TO N-ACETYLGLUTAMATE SYNTHETASE DEFICIENCY *237450 : HYPERBILIRUBINEMIA, ROTOR TYPE *237800 : HYPERBILIRUBINEMIA, SHUNT *238300 : HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE I *238310 : HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE II *238320 : HYPERGONADOTROPIC HYPOGONADISM; HHG *238330 : HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE III *238331 : GLYCINE CLEAVAGE SYSTEM L PROTEIN; GCSL *238600 : HYPERLIPOPROTEINEMIA, TYPE I *238700 : HYPERLYSINEMIA *239000 : HYPEROSTOSIS CORTICALIS DEFORMANS JUVENILIS *239100 : HYPEROSTOSIS CORTICALIS GENERALISATA *239300 : HYPERPHOSPHATASIA WITH MENTAL RETARDATION *239500 : HYPERPROLINEMIA, TYPE I *239510 : HYPERPROLINEMIA, TYPE II *239800 : HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME *240200 : HYPOADRENOCORTICISM, FAMILIAL *240300 : AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I *240500 : COMMON VARIABLE IMMUNODEFICIENCY *241080 : HYPOGONADISM, DIABETES MELLITUS, ALOPECIA, MENTAL RETARDATION, AND ELECTROCARDIOGRAPHIC ABNORMALITIES *241150 : HYPOKALEMIA, FAMILIAL *241310 : HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS *241400 : HYPOPARATHYROIDISM *241410 : HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRD *241530 : HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY; HHRH *241900 : HYPOTRICHOSIS *242500 : ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE *242600 : IMINOGLYCINURIA *242650 : IMMOTILE CILIA SYNDROME 1; ICS1 *242670 : IMMOTILE CILIA SYNDROME DUE TO DEFECTIVE RADIAL SPOKES *242700 : IMMUNE DEFECT DUE TO ABSENCE OF THYMUS *242860 : IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME *242900 : IMMUNOOSSEOUS DYSPLASIA *243000 : INDIFFERENCE TO PAIN *243150 : INTESTINAL ATRESIA, MULTIPLE *243180 : INTESTINAL PSEUDOOBSTRUCTION DUE TO NEURONAL DISEASE *243305 : INVERSIN *243400 : ISONIAZID INACTIVATION *243500 : ISOVALERICACIDEMIA; IVA *243600 : JEJUNAL ATRESIA *243800 : JOHANSON-BLIZZARD SYNDROME; JBS *244200 : KALLMANN SYNDROME 3; KAL3 *244400 : KARTAGENER SYNDROME *244450 : KAUFMAN OCULOCEREBROFACIAL SYNDROME *244460 : KENNY-CAFFEY SYNDROME, TYPE 1; KCS *245000 : PAPILLON-LEFEVRE SYNDROME; PALS *245010 : KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA AND ONYCHOGRYPOSIS *245050 : 3-@OXOACID CoA TRANSFERASE; OXCT *245100 : KETOACIDURIA WITH MENTAL DEFICIENCY AND OTHER FEATURES *245200 : KRABBE DISEASE *245349 : PYRUVATE DEHYDROGENASE COMPLEX, COMPONENT X *245400 : LACTIC ACIDOSIS, CONGENITAL INFANTILE *245480 : LACTOFERRIN-DEFICIENT NEUTROPHILS *245600 : LARSEN SYNDROME, RECESSIVE *245660 : LARYNGOONYCHOCUTANEOUS SYNDROME; LOCS *245800 : LAURENCE-MOON SYNDROME *245900 : LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY *246000 : LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT *246400 : LETTERER-SIWE DISEASE *246450 : 3-@HYDROXY-3-METHYLGLUTARYL-COENZYME A LYASE DEFICIENCY *246530 : LEUKOTRIENE C4 SYNTHASE; LTC4S *246600 : LIPASE, CONGENITAL ABSENCE OF PANCREATIC *246700 : LIPID TRANSPORT DEFECT OF INTESTINE *246800 : LIPIDOSIS, JUVENILE DYSTONIC *246900 : LIPOAMIDE DEHYDROGENASE DEFICIENCY, LACTIC ACIDOSIS DUE TO *247100 : LIPOID PROTEINOSIS OF URBACH AND WIETHE *247800 : LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNE HEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS *247980 : LIPASE B, LYSOSOMAL ACID; LIPB *248300 : MAL DE MELEDA *248310 : MALARIA, INTENSITY OF INFECTION IN *248360 : MALONYL CoA DECARBOXYLASE DEFICIENCY *248370 : MANDIBULOACRAL DYSPLASIA; MAD *248500 : MANNOSIDOSIS, ALPHA B, LYSOSOMAL *248510 : MANNOSIDOSIS, BETA; MANB1 *248600 : MAPLE SYRUP URINE DISEASE, TYPE IA *248610 : MAPLE SYRUP URINE DISEASE, TYPE II *248611 : MAPLE SYRUP URINE DISEASE, TYPE IB *248700 : MARDEN-WALKER SYNDROME *248800 : MARINESCO-SJOGREN SYNDROME; MSS *248900 : MAST SYNDROME *249000 : MECKEL SYNDROME; MKS *249100 : MEDITERRANEAN FEVER, FAMILIAL; MEFV *249210 : MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME *249310 : MEGALOCORNEA-MENTAL RETARDATION SYNDROME *249620 : MENTAL RETARDATION, CONGENITAL HEART DISEASE, BLEPHAROPHIMOSIS, BLEPHAROPTOSIS, AND HYPOPLASTIC TEETH *249650 : MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU *250100 : METACHROMATIC LEUKODYSTROPHY *250250 : CARTILAGE-HAIR HYPOPLASIA; CHH *250600 : METATROPIC DWARFISM *250620 : METHACRYLICACIDURIA *250790 : METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5 *250800 : METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE *250850 : METHIONINE ADENOSYLTRANSFERASE DEFICIENCY *250900 : METHIONINE MALABSORPTION SYNDROME *250950 : 3-@METHYLGLUTACONICACIDURIA *251000 : METHYLMALONICACIDURIA DUE TO METHYLMALONIC CoA MUTASE DEFICIENCY *251100 : METHYLMALONICACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMINcbl A *251110 : METHYLMALONICACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMINcbl B *251170 : MEVALONATE KINASE; MVK *251200 : MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE 1; MCPH1 *251230 : MICROCEPHALY-MICROMELIA SYNDROME *251270 : MICROCEPHALY WITH CHORIORETINOPATHY *251300 : MICROCEPHALY, HIATUS HERNIA, AND NEPHROTIC SYNDROME *251450 : MICROMELIC DWARFISM WITH VERTEBRAL AND METAPHYSEAL ABNORMALITIES AND ADVANCED CARPOTARSAL OSSIFICATION *251500 : MICROPHTHALMIA AND MENTAL DEFICIENCY *251600 : MICROPHTHALMOS, AUTOSOMAL RECESSIVE *251800 : MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS *251850 : MICROVILLUS INCLUSION DISEASE *252100 : MOHR SYNDROME *252350 : MOYAMOYA DISEASE *252500 : MUCOLIPIDOSIS II *252600 : MUCOLIPIDOSIS III *252605 : MUCOLIPIDOSIS III, VARIANT FORM *252650 : MUCOLIPIDOSIS IV *252800 : MUCOPOLYSACCHARIDOSIS TYPE I *252900 : MUCOPOLYSACCHARIDOSIS TYPE IIIA *252920 : MUCOPOLYSACCHARIDOSIS TYPE IIIB *252930 : MUCOPOLYSACCHARIDOSIS TYPE IIIC *252940 : MUCOPOLYSACCHARIDOSIS TYPE IIID *253000 : MUCOPOLYSACCHARIDOSIS TYPE IVA *253200 : MUCOPOLYSACCHARIDOSIS TYPE VI *253220 : MUCOPOLYSACCHARIDOSIS TYPE VII *253240 : MUCUS INSPISSATION OF RESPIRATORY TRACT *253250 : MULIBREY NANISM; MUL *253260 : BIOTINIDASE; BTD *253270 : MULTIPLE CARBOXYLASE DEFICIENCY, BIOTIN-RESPONSIVE; MCD *253280 : MUSCLE-EYE-BRAIN DISEASE; MEB *253290 : MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE *253310 : LETHAL CONGENITAL CONTRACTURE SYNDROME *253700 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C *253800 : FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY; FCMD *253900 : MUSCULAR DYSTROPHY, CONGENITAL, PRODUCING ARTHROGRYPOSIS *254110 : MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H *254150 : MUSK, INABILITY TO SMELL *254210 : MYASTHENIA GRAVIS, FAMILIAL INFANTILE; FIMG *254600 : MYELOPEROXIDASE DEFICIENCY *254770 : MYOCLONIC EPILEPSY, JUVENILE; EJM1 *254780 : EPILEPSY, PROGRESSIVE MYOCLONIC 2; EPM2A *254900 : MYOCLONUS-NEPHROPATHY SYNDROME *255125 : MYOPATHY WITH DEFICIENCY OF SUCCINATE DEHYDROGENASE AND ACONITASE *255300 : MYOPATHY, CONGENITAL *255320 : MYOPATHY, CONGENITAL MULTICORE, WITH EXTERNAL OPHTHALMOPLEGIA *255800 : SCHWARTZ-JAMPEL SYNDROME; SJS *255960 : MYXOMA, INTRACARDIAC *256100 : NEPHRONOPHTHISIS, FAMILIAL JUVENILE 1; NPHP1 *256500 : NETHERTON DISEASE *256520 : NEU-LAXOVA SYNDROME; NLS *256540 : NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY *256550 : NEURAMINIDASE DEFICIENCY *256600 : NEUROAXONAL DYSTROPHY, INFANTILE *256700 : NEUROBLASTOMA *256710 : NEUROECTODERMAL MELANOLYSOSOMAL DISEASE *256731 : CEROID LIPOFUSCINOSIS, NEURONAL 5; CLN5 *256810 : NEUROPATHY, CONGENITAL SENSORY, WITH NEUROTROPHIC KERATITIS *256850 : NEUROPATHY, GIANT AXONAL; GAN *256855 : NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL RECESSIVE *257150 : NEUTROPHIL ACTIN DYSFUNCTION; NAD *257200 : NIEMANN-PICK DISEASE *257220 : NIEMANN-PICK DISEASE, TYPE C *257270 : NIGHT BLINDNESS WITH HIGH-GRADE MYOPIA *257320 : NORMAN-ROBERTS LISSENCEPHALY SYNDROME *257550 : OCULAR MOTOR APRAXIA *257600 : OCULAR MYOPATHY WITH CURARE SENSITIVITY *257800 : OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION *257850 : OCULODENTOOSSEOUS DYSPLASIA, RECESSIVE *257970 : OCULORENOCEREBELLAR SYNDROME *258120 : OHAHA SYNDROME *258150 : OLIGOSYNAPTIC INFERTILITY *258300 : OLIVOPONTOCEREBELLAR ATROPHY II *258360 : ONYCHOTRICHODYSPLASIA AND NEUTROPENIA *258400 : OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS *258480 : OPSISMODYSPLASIA *258501 : OPTIC ATROPHY 3; OPA3 *258700 : OPTICOCOCHLEODENTATE DEGENERATION *258850 : ORAL-FACIAL-DIGITAL SYNDROME, TYPE III *258870 : ORNITHINE AMINOTRANSFERASE DEFICIENCY *258900 : OROTICACIDURIA I *259250 : OSTEODYSPLASIA, FAMILIAL, ANDERSON TYPE *259450 : BRUCK SYNDROME *259700 : OSTEOPETROSIS, AUTOSOMAL RECESSIVE *259730 : OSTEOPETROSIS WITH RENAL TUBULAR ACIDOSIS *259770 : OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG *259780 : OTOONYCHOPERONEAL SYNDROME *259900 : OXALOSIS I *260000 : OXALOSIS II *260005 : 5-@OXOPROLINASE DEFICIENCY *260300 : PALLIDOPYRAMIDAL SYNDROME *260400 : PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION *260565 : PEHO SYNDROME *260600 : PELIZAEUS-MERZBACHER DISEASE, ACUTE INFANTILE TYPE *260800 : PENTOSURIA *261000 : PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR *261510 : PEROXISOMAL 3-OXOACYL-COENZYME A THIOLASE DEFICIENCY *261515 : PEROXISOMAL BIFUNCTIONAL ENZYME DEFICIENCY *261540 : PETERS ANOMALY WITH SHORT-LIMB DWARFISM *261600 : PHENYLKETONURIA *261630 : PHENYLKETONURIA II *261640 : 6-@PYRUVOYLTETRAHYDROPTERIN SYNTHASE; PTS *261650 : PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL; PCK2 *261670 : PHOSPHOGLYCERATE MUTASE, DEFICIENCY OF M SUBUNIT OF *261680 : PHOSPHOENOLPYRUVATE CARBOXYKINASE 1, SOLUBLE; PCK1 *261750 : PHOSPHORYLASE KINASE DEFICIENCY OF LIVER AND MUSCLE *262000 : PILI TORTI AND NERVE DEAFNESS *262300 : ACHROMATOPSIA 3; ACHM3 *262600 : PITUITARY DWARFISM III *262850 : PLASMIN INHIBITOR DEFICIENCY *263000 : PNEUMONITIS, FAMILIAL DESQUAMATIVE INTERSTITIAL; DIP *263200 : POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1 *263210 : POLYCYSTIC KIDNEY DISEASE, POTTER TYPE I, WITH MICROBRACHYCEPHALY, HYPERTELORISM, AND BRACHYMELIA *263400 : ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN *263520 : POLYDACTYLY WITH NEONATAL CHONDRODYSTROPHY, TYPE II *263530 : POLYDACTYLY WITH NEONATAL CHONDRODYSTROPHY, TYPE I *263570 : POLYGLUCOSAN BODY DISEASE, ADULT FORM; APBD *263650 : POPLITEAL PTERYGIUM SYNDROME, LETHAL TYPE *263700 : PORPHYRIA, CONGENITAL ERYTHROPOIETIC *263750 : POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS *264080 : PROGESTERONE RESISTANCE; PGR *264090 : PROGEROID SYNDROME, NEONATAL *264270 : PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES *264300 : PSEUDOHERMAPHRODITISM, MALE, WITH GYNECOMASTIA *264450 : PSEUDOMONGOLISM *264470 : PSEUDONEONATAL ADRENOLEUKODYSTROPHY *264600 : PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH *264700 : PSEUDOVITAMIN D DEFICIENCY RICKETS *264800 : PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL RECESSIVE; PXE *264900 : PTA DEFICIENCY *265000 : PTERYGIUM SYNDROME *265100 : PULMONARY ALVEOLAR MICROLITHIASIS *265900 : PYLE DISEASE *265950 : PYLORIC ATRESIA *266100 : PYRIDOXINE DEPENDENCY WITH SEIZURES *266120 : PYRIMIDINE NUCLEOTIDASE DEFICIENCY, HEMOLYTIC ANEMIA FROM *266150 : PYRUVATE CARBOXYLASE DEFICIENCY *266200 : PYRUVATE KINASE DEFICIENCY OF ERYTHROCYTE *266250 : RADICULONEUROPATHY, FATAL NEONATAL *266265 : LEUKOCYTE ADHESION DEFICIENCY, TYPE II *266300 : HAIR COLOR 2; HCL2 *266350 : RED SKIN PIGMENT ANOMALY OF NEW GUINEA *266600 : INFLAMMATORY BOWEL DISEASE 1; IBD1 *266900 : RENAL DYSPLASIA AND RETINAL APLASIA *267000 : RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM *267430 : RENAL TUBULAR DYSGENESIS *267500 : RETICULAR DYSGENESIA *267750 : KNOBLOCH SYNDROME; KNO *268080 : RETINOSCHISIS OF FOVEA *268100 : RETINOSCHISIS WITH EARLY HEMERALOPIA *268200 : RHABDOMYOLYSIS, ACUTE RECURRENT *268300 : ROBERTS SYNDROME; RBS *268310 : ROBINOW SYNDROME, RECESSIVE FORM *268800 : SANDHOFF DISEASE *268900 : SARCOSINEMIA *269250 : SCHNECKENBECKEN DYSPLASIA *269500 : SCLEROSTEOSIS *269700 : BERARDINELLI-SEIP CONGENITAL LIPODYSDROPHY; BSCL *269860 : SHORT RIB SYNDROME, BEEMER TYPE *269920 : SIALIC ACID STORAGE DISEASE; SIASD *270100 : SITUS INVERSUS VISCERUM *270200 : SJOGREN-LARSSON SYNDROME *270300 : SKIN PEELING, FAMILIAL CONTINUOUS *270550 : SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE; SACS *270600 : SPASTIC DIPLEGIA, INFANTILE TYPE *270685 : SPASTIC PARAPARESIS WITH AMYOTROPHY OF HANDS AND FEET *270700 : SPASTIC PARAPLEGIA AND RETINAL DEGENERATION *270800 : SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A *271245 : INFANTILE-ONSET SPINOCEREBELLAR ATAXIA; IOSCA *271400 : SPLENIC HYPOPLASIA *271550 : SPONDYLOENCHONDRODYSPLASIA *271600 : SPONDYLOEPIPHYSEAL DYSPLASIA TARDA *271630 : SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE *271640 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY; SEMDJL *271650 : SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE; SEMDIT *271900 : CANAVAN DISEASE *271980 : ALDEHYDE DEHYDROGENASE 5 FAMILY, MEMBER A1; ALDH5A1 *272200 : MULTIPLE SULFATASE DEFICIENCY *272300 : SULFOCYSTEINURIA *272370 : SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS; EC1 *272460 : SYNSPONDYLISM, CONGENITAL *272650 : TATSUMI FACTOR DEFICIENCY *272750 : TAY-SACHS DISEASE, AB VARIANT *272800 : TAY-SACHS DISEASE; TSD *273300 : TESTICULAR TUMORS *273395 : TETRA-AMELIA WITH PULMONARY HYPOPLASIA *273750 : THREE M SYNDROME *273800 : THROMBASTHENIA OF GLANZMANN AND NAEGELI *273900 : THROMBOCYTOPENIA *274000 : THROMBOCYTOPENIAABSENT RADIUS SYNDROME *274150 : THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL *274180 : THROMBOXANE A SYNTHASE 1; TBXAS1 *274190 : THUMB AGENESIS, DWARFISM, AND IMMUNODEFICIENCY *274270 : DIHYDROPYRIMIDINE DEHYDROGENASE; DPYD *274500 : THYROID HORMONOGENESIS, GENETIC DEFECT IN, IIA *274600 : PENDRED SYNDROME; PDS *274700 : THYROID HORMONOGENESIS, GENETIC DEFECT IN, III *274800 : THYROID HORMONOGENESIS, GENETIC DEFECT IN, IV *275120 : THYROTROPIN-RELEASING HORMONE DEFICIENCY *275210 : TIGHT SKIN CONTRACTURE SYNDROME, LETHAL *275250 : TONGUE, PIGMENTED FUNGIFORM PAPILLAE OF *275350 : TRANSCOBALAMIN II DEFICIENCY *275355 : TRANSFORMING GROWTH FACTOR, BETA-1 RESPONSE ELEMENT *275360 : TREHALASE *275370 : TRICARBOXYLIC ACID CYCLE, DEFECT OF *275630 : TRIGLYCERIDE STORAGE DISEASE WITH IMPAIRED LONG-CHAIN FATTY ACID OXIDATION *275900 : TROYER SYNDROME *276000 : PROTEASE, SERINE, 1; PRSS1 *276100 : TRYPTOPHANURIA WITH DWARFISM *276600 : TYROSINE TRANSAMINASE DEFICIENCY *276700 : TYROSINEMIA, TYPE I *276710 : TYROSINEMIA, TYPE III *276820 : ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY *276900 : USHER SYNDROME, TYPE IA; USH1A *276901 : USHER SYNDROME, TYPE IIA; USH2A *276902 : USHER SYNDROME, TYPE III; USH3 *276903 : MYOSIN VIIA; MYO7A *276904 : USHER SYNDROME, TYPE IC; USH1C *276905 : USHER SYNDROME, TYPE IIB; USH2B *277100 : VALINEMIA *277150 : VAN BOGAERT-HOZAY SYNDROME *277170 : VARADI-PAPP SYNDROME *277300 : SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE, 1 *277320 : VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA *277350 : VITAMIN A METABOLIC DEFECT *277400 : VITAMIN B12 METABOLIC DEFECT WITH METHYLMALONICACIDEMIA AND HOMOCYSTINURIA *277410 : VITAMIN B12 METABOLIC DEFECT, TYPE 2 *277470 : VOLENDAM NEURODEGENERATIVE DISEASE *277600 : WEILL-MARCHESANI SYNDROME *277700 : WERNER SYNDROME; WRN *277730 : WERNICKE-KORSAKOFF SYNDROME *277900 : WILSON DISEASE *277950 : WINCHESTER DISEASE *278000 : WOLMAN DISEASE *278250 : WRINKLY SKIN SYNDROME; WSS *278300 : XANTHINURIA, TYPE I *278700 : XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA *278720 : XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC *278740 : XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E

63. Thoms Community Care Foundation Nellie's condition is known as anophthalmos; about one child in amillion is born with it. Bilateral anophthalmos missing both http://www.thomsfoundation.org/friends.html

About TCCF Stories • Finding Friends • Diff. a Day Makes ... Home On October 20, 1993, a baby girl was born to Nadia and Victor Kuzmich in Moscow, Russia. She was born without eyes and only the merest slits where her eyes should have been. Her parents named her Nellie. They knew at birth what life held for Nellie in Russia. She would live with her parents for as long as they lived. There would be no school, no therapies, no special services. All that could be done in Russia was the form small eye pockets and, at one month, to give Nellie her first prosthetic eyes which would be changed regularly so her sockets could grow as they naturally should. Wondering what the future might hold for Nellie, her mother recalled, "We heard America was great." In 1997, the Kuzmichs brought Nellie and their son, Dennis, to Asheville where Victor's brother lived. For five months, every day, sometimes twice a day, they visited doctors, community services and therapists of every description. Nellie's condition is known as anophthalmos; about one child in a million is born with it. Bilateral anophthalmos - missing both eyes - is even more rare; Nellie is likely the only child in North Carolina with the condition. Insurance didn't cover prosthetic eyes for Nellie. Neither did Medicaid. For a long time, NC Services for the Blind helped with Nellie's prosthetic eyes, which by that time changed every six months. But as Victor Kuzmich began to find his professional niche in America, Nellie ceased to qualify for blind services aid. The prosthetics cost $3,600 a pair - every six months. And Nellie required other therapies.

64. New Page 5 BBC) had developed the high temperature treated human bone hydroxyapatite intraorbitalimplant (HHAOI) to be used as a cosmetic correction for anophthalmos. http://members.tripod.com/biothai/haoi.htm

RECONSTRUCTION SURGERY INTRODUCTION 1. Very rare possibility of fibrosis or rejection 2. During the placement of the eye ball surface prosthesis, the intra ocular implant will provide a very stable seating bed. 3. The ends of the dura can be convinently attached to the 6 muscles in the eye which will results in the optimally co-ordinated eye ball movement with respect to the normal eye. PATIENT DETAILS Patient Name : Mr. Jigong Moddang Surgeon Name : Dr. Chalao Hospital Name : Bangkok Priest hospital Patient Age : 69 years Diagnosis : Phthisis bulbi RE / Shallow fornix RE Date of Surgery : 14/03/2000 Post operative one week with human hydroxyapatite X-ray post operative one week Case No. 2 post operative one week. Post operative one week Case Report: Application of High Temperature Treated Human Bone Hydroxyapatite Intra Orbital Implant Wrapped in Dura mater in Ophthalmology. Abstract Orbital implants may be divided into three groups: the buried nonintegrated, the buried integrated and the exposed integrated implants. The motility of the prosthesis with the buried nonintegrated implants, such as the Mule’s sphere implant, is generally poor. Although Nunery and associates

65. Tips For Printing Hydrocephaly, 16, 4, nr, 7.68, NA. Total anophthalmos / Microphthalmos(include unspecified) (2), 5, 0, nr, 1.92, NA. anophthalmos (2), 1, 0,nr, 0.38, NA. http://ibis-birthdefects.org/start/ukbdrate.htm

Tips for printing BIRTH DEFECTS (BD) RATES IN UKRAINE About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Data for 2000 (Rivne and Volyn oblasts) Live births (L) Stillbirths (S) Total births Number of terminations of pregnancy (ToP) for birth defects (1) Birth Defects Number of cases Rates * 10000 Livebirths Stillbirths ToP* L+S L+S+ToP Anencephaly N.A. Spina bifida N.A. Encephalocele N.A. Microcephaly (2) nr N.A. Arhinencephaly / Holoprosencephaly nr N.A. Hydrocephaly nr N.A. Total Anophthalmos / Microphthalmos (include unspecified) (2) nr N.A. Anophthalmos (2) nr N.A. Microphthalmos (2) nr N.A. Total Anotia / Microtia (include unspecified) nr N.A. Anotia nr N.A. Microtia nr N.A. Transposition of great vessels nr N.A. Tetralogy of Fallot nr N.A. Hypoplastic left heart syndrome nr N.A. Coarctation of aorta nr N.A. Choanal atresia, bilateral nr N.A. Cleft palate without cleft lip nr N.A. Cleft lip with or without cleft palate nr N.A.

66. Primary Embryonic Stage Results Congenital Anomalies Primary Embryonic Stage (True anophthalmos),Primary Embryonic Stage (True anophthalmos). When the http://www.jahrling.com/Result/Case1-1.htm

Visually Impaired Link Results Congenital Anomalies Primary Embryonic Stage (True Anophthalmos) When the congenital anomaly is the absence of an eye and/or partially formed eyelids it is far more complex to manage, because the bony orbital wall and facial features never completely developed. Our method of non-surgical augmentation of the orbital area and the eyelid aperture (with pressure stem conformers) is an accepted standard of treatment, and is practiced by other Board Certified Ocularists and members of the American Society of Ocularists. Because of the number of laboratory fitting sessions and the length of time it takes before the first ocular prosthesis is fitted, it is recommended parents seek this service from an ocularist close to their home. This first case presents bilateral narrow bony orbital walls with micro-eyelids that were slit-like, firm and taut, with entropion (inversion) of the lower eyelids and lashes. When the eyelids are separated there is no eyeball present and the socket is funnel shaped lacking definition of culs-de-sac or fornices (internal eyelid formation). This is the earliest of prenatal stage aberrations. The cavity will neither retain nor self-support any type of prosthetic device without first applying (long-term) external force to the orbital void with empirically fitting a series of incremental sized and shaped pressure stem conformers. The object its to gradually expand the eyelid aperture while trying to create fornices (the under part of the eyelid). The projected time span before an ocular prosthesis can be retained is usually 1 to 3 years.

67. Glossary Of Ocular Terminology Anophthalmic/anophthalmos Absence of an eye(s). It can be a congenital(born without) or an acquired condition (surgically removed). http://www.jahrling.com/Reference/Glossary.htm

Visually Impaired Link Glossary Terminology and Definitions A B C D ... T Anophthalmic/Anophthalmos Absence of an eye(s). It can be a congenital (born without) or an acquired condition (surgically removed). Acquired Condition A condition that can be brought about by an eye disease, trauma or surgery resulting in phthisis evisceration enucleation or exenteration of the eye. Adipose Tissue Orbital fatty tissue that cushions the eyeball. lt is usually made reference to when its loss, reduction or displacement within the orbit causes facial asymmetry of the eyelids resulting in enophthalmos and/or superior sulcus depression. Adiposis The breaking down of fatty tissue, or its gravitational displacement following loss of the eye. It can also occur following trauma induced phthisis Adnexa Appendages of the eyeball, which includes the eyelids, muscles and soft tissue. Alginate A powdery extract of marine kelp when mixed with water sets into a gelatinous form. It is used to taking impressions of the orbit or globe. Anterior Chamber Area between the cornea and iris in both the human eye and the ocular prosthesis.

68. Oculoplastic Surgery - Reconstructive Surgery - VisionChannel A child born without an eyeball (congenital anophthalmos) usually has a smalleye socket (orbit) because normal development did not take place in utero. http://www.visionchannel.net/oculoplasticsurgery/reconstructive.shtml

Home Search SiteMap Ask the Dr. ... Medical Store advertisement OCULOPLASTIC SURGERY Overview Cosmetic Surgery Corrective Surgery Repair of Eyelid Malpositions Reconstructive Surgery Orbital Decompression Enucleation Implantation CONDITIONS Amblyopia (lazy eye) Blepharitis Cataracts Color Vision Deficiency ... Refractive Errors Correction Retinal Detachment Retinitis Pigmentosa Retinopathy of Prematurity Skin Cancer of the Eyelids Tear Duct Obstruction INTERACT VisionForum Links Clinical Trials ABOUT US Healthcommunities.com Pressroom Bibliography Reconstructive Surgery Surgical removal of skin cancer of the eyelid is standard therapy. Depending on the size, depth, and location of the lesion, this can cause substantial loss of eyelid skin that may affect its function and appearance. Surgeons attempt to preserve as much skin as possible and minimize scarring, while making sure that all of the cancer cells are removed. Moh’s technique, (link) or frozen section control, for example, enables the surgeon to excise the tumor while leaving more healthy tissue intact. Some very small tumors may heal on their own, through a process called granulation A large tumor may require reconstructive surgery. Two methods used are

69. Select Entries From OMIM -- Online Mendelian Inheritance In Man ANOMALIES 156900 MICROPHTHALMOS WITH MYOPIA AND CORECTOPIA *251500 MICROPHTHALMIAAND MENTAL DEFICIENCY *309800 MICROPHTHALMIA OR anophthalmos, WITH ASSOCIATED http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/eye/microphthalmos.htm

Select Entries from OMIM Online Mendelian Inheritance in Man Back to Senses Abnormalities 32 entries found, searching for "microphthalmos" NANOPHTHALMOS 1; NNO1 MICROPHTHALMOS, AUTOSOMAL RECESSIVE LYMPHEDEMA, MICROCEPHALY, CHORIORETINOPATHY SYNDROME MICROPHTHALMOS, PIGMENTARY RETINOPATHY, AND GLAUCOMA TACHYCARDIA, HYPERTENSION, MICROPHTHALMOS, AND HYPERGLYCINURIA RODRIGUES BLINDNESS MICROPHTHALMOS WITH HYPERMETROPIA, RETINAL DEGENERATION, MACROPHAKIA AND DENTAL ANOMALIES MICROPHTHALMOS WITH MYOPIA AND CORECTOPIA MICROPHTHALMIA AND MENTAL DEFICIENCY MICROPHTHALMIA OR ANOPHTHALMOS, WITH ASSOCIATED ANOMALIES; MAA REESE RETINAL DYSPLASIA CATARACT, CONGENITAL, CERULEAN TYPE, 2; CCA2 RIEGER SYNDROME, TYPE 1; RIEG1 ANOPHTHALMIA AND ESOPHAGEAL ATRESIA CATARACT, CONGENITAL, CERULEAN TYPE, 1; CCA1 COLOBOMA, UVEAL, WITH CLEFT LIP AND PALATE AND MENTAL RETARDATION CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES; CCT OCULODENTODIGITAL DYSPLASIA; ODDD FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA CATARACT, MICROPHTHALMIA, AND NYSTAGMUS

70. Select Entries From OMIM -- Online Mendelian Inheritance In Man WITH OTHER MALFORMATIONS *123570 CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED200110 ABLEPHARONMACROSTOMIA SYNDROME *206900 anophthalmos, TRUE OR http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/eye/cryptophthalmos.htm

Select Entries from OMIM Online Mendelian Inheritance in Man Back to Senses Abnormalities 5 entries found, searching for "cryptophthalmos" CRYPTOPHTHALMOS WITH OTHER MALFORMATIONS CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED ABLEPHARON-MACROSTOMIA SYNDROME ANOPHTHALMOS, TRUE OR PRIMARY ANOPHTHALMOS, CLINICAL; ANOP1

71. JASI : Journal Of The Anatomical Society Of India In our case, the baby had anophthalmos, syndactyly and ambiguous genitalia as majorand congenital malformations of nose, ears, skeletal defects and renal http://www.jasi.net/june2002/syndrome.html

Editorial Board Home About Us Contact Us ... Feedback J Anat. Soc. India Vol. 51 (1) 59-60 (June 2002) Fraser Syndrome With Unusual Features—A Case Report Mahadevan , B; * Bhat , B.V; * Sastri , A.T; ** Rao , S; ** Kusre , G. Department of * Paediatrics Pondicherry INDIA Abstract. Fraser Syndrome is a rare autosomal recessive disorder characterized by partial webbing of the fingers and toes (partial syndactyly ), renal abnormalities, genital malformations and/or, in some cases, complete fusion of the eyelids ( cryptophthalmos ). A preterm child with Fraser syndrome presenting with unusual abnormalities is reported. Key words crytopthalmos syndrome anophthalmia Introduction : Fraser (1962) described the first report of autosomal recessive cryptophthalmos syndrome Francois (1969) observed the main features to be crytophthalmos , anomalies of the hand, ears, nose, syndactyly , and genital abnormalities.

72. Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : A Diseases Da degeneration see Senile macular retinal degeneration Agenesis of corpus callosumsee Corpus callosum hypoplasia Agenesis of eye see anophthalmos Ageusia see http://www.diseasesdatabase.com/sieve/disease_index_a.asp

Diseases Database [Previous page] [Search] [Index] [Feedback] Diseases Database disease, symptom, sign, etc alphabetical index : A AA amyloidosis Aagenaes syndrome see Cholestasis-oedema syndrome, Norwegian type Aarskog Ose Pande syndrome see SHORT syndrome Aarskog syndrome Aarskog-Scott syndrome see Aarskog syndrome Aase syndrome Abacavir Abciximab Abdo distended see Abdominal distention Abdo mass see Abdominal mass Abdo pain see Abdominal pain Abdomen distended see Abdominal distention Abdominal and pelvic pain see Abdominal pain Abdominal decompression Abdominal distention Abdominal mass Abdominal obesity-metabolic syndrome see Reaven syndrome X Abdominal pain Abdominal swelling see Abdominal distention Abducens nerve lesion see 6th cranial nerve disorder Abducent nerve pathology see 6th cranial nerve disorder Abetalipoproteinaemia Abetalipoproteinemia see Abetalipoproteinaemia Abnormal heart rhythm see Cardiac arrhythmia Abnormal heart sounds Abnormal reflexes Abnormal splitting of heart sounds ... Abnormal sputum ABO incompatibility (feto-maternal) see ABO isoimmunization of fetus and newborn ABO isoimmunization of fetus and newborn Abortion, missed

73. Osmed Gmbh For some indications osmed has the approval CEmark in Europe for radialis flap,anophthalmos and secondary breast reconstruction; in the USA the 510k for http://www.osmed.biz/html_e/produkte/produkte.html

Products Osmosis expanders for tissue expansion are stable, mainly dry devices, made of a crosslinked, physiologically well tolerated hydrogel (co-polymere based on Methylmethacrylate and N-vinylpyrrolidone). After implantation body fluid is absorbed from the surrounding tissue by osmosis. The volume of the implant is thereby increased 3 to 12 fold. The expanded tissue serves as a receptacle for a permanent implant or as material to cover defects. Osmosis Expander before and after swelling Advantages

74. Administrative Staff College Of India; Dandona; ASCI Hornby SJ, Dandona L, Foster A, Jones RB, Gilbert CE. Clinical findings, consanguinity,and pedigrees in children with anophthalmos in southern India. http://www.asci.org.in/faculty/dandona_pubs.html

Dr. Lalit Dandona Publications up to December 2002 Publications in journals: Dandona L. HIV/AIDS control in India. Lancet Dandona L. Conceptualizing health policy. National Medical Journal of India Dandona L, Dandona R, John RK. Estimation of blindness in India from 2000 through 2020: Implications for the blindness control policy. National Medical Journal of India Dandona L. Blindness control in India: beyond anachronism. [invited article] Lancet Dandona L. Medical migration. Lancet Dandona L, Dandona R, Naduvilath TJ, McCarty CA, Nanda A, Srinivas M, Mandal P, Rao GN. Is current eye-care-policy focus almost exclusively on cataract adequate to deal with blindness in India? Lancet Dandona L. Improving health in India. Lancet Dandona L. Outcome of cataract surgery is poor in developing countries. British Medical Journal Dandona R, Dandona L. Why do we overlook data from our own country? National Medical Journal of India Dandona R, Dandona L, Srinivas M, Sahare P, Narsaiah S, Munoz SR, Pokharel GP, Ellwein LB. Refractive error in children in a rural population in India. Investigative Ophthalmology and Visual Science Dandona R, Dandona L, Srinivas M, Giridhar P, Prasad MN, Vilas K, McCarty CA, Rao GN. Moderate visual impairment in India: the Andhra Pradesh Eye Disease Study.

75. Isurgeon -- Case Discussion Board: Lid And Adnexa Daljit Singh (Added 25Sep-2000 Hits 21). anophthalmos - 16 years old femalewith congenital unilateral anophthalmos, now facing cosmetic problems. http://www.isurgeon.org/wwwboard/cat/Lid_and_Adnexa/

A Isurgeon Case Discussion Board: Lid and Adnexa Top : Lid and Adnexa Discussion: - Dear Dr.Mandar Paranjpe, The best surgical management for involutional entropion I believe would depend on the mechanics in play. If the mechanism is predominantly lid laxity one may aim for a simple lateral tarsal strip procedure. One may need to simultaneously restore retractor action in which case a good option would be to open the lower lid with a blepharoplasty incision and explore-identifying-reattaching/plicating the retractors. During this stage of the procedure any coexisting orbicularis override can also be dealt with by stripping a sliver of orbicularis. I think this sequence of surgical options is superior to adopting standard procedures like Weiss/Jones etc since it aims to address the mechanics of the entropion that may be in play in the individual cases. With regards to the second question the best choice of treatment would again depend on the situation. If it is a one off ptoblem one could simply epilate and treat any associated problems like blepharitis. If recurrent - options available are electrolysis, laser, cryo. These are more permanent. Beware use of drops like latanoprost which may be the cause. I hope this helps new (Added: 20-Mar-2003 Hits: 1) Acute lid/orbital pain she was treated with antibiotics, nsaids.she was ok after this t/t

76. ICD-9-CM Congenital Anomalies Codes 7429, NERVOUS SYSTEM ANOM NOS. 743, CONGENITAL EYE ANOMALY*. 7430, anophthalmos*.74300, CLINIC anophthalmos NOS. 74303, CONGEN CYSTIC EYEBALL. 74306, CRYPTOPHTHALMOS. http://www.health.state.ok.us/program/hci/icd9v16/congenital.html

Congenital Anomalies * Indicates a code category. Not a valid reporting code. Code Description ANENCEPHALUS/SIMIL ANOM* ANENCEPHALUS CRANIORACHISCHISIS INIENCEPHALY SPINA BIFIDA* SPINA BIF W HYDROCEPHAL* SPIN BIF W HYDROCEPH NOS SPIN BIF W HYDRCEPH-CERV SPIN BIF W HYDRCEPH-DORS SPIN BIF W HYDRCEPH-LUMB SPINA BIFIDA* SPINA BIFIDA SPINA BIFIDA-CERV SPINA BIFIDA-DORSAL SPINA BIFIDA-LUMBAR OTH NERVOUS SYSTEM ANOM* ENCEPHALOCELE MICROCEPHALUS REDUCTION DEFORM, BRAIN CONGENITAL HYDROCEPHALUS BRAIN ANOMALY NEC SPINAL CORD ANOMALY NEC* DIASTEMATOMYELIA HYDROMYELIA SPINAL CORD ANOMALY NEC NERVOUS SYSTEM ANOM NEC NERVOUS SYSTEM ANOM NOS CONGENITAL EYE ANOMALY* ANOPHTHALMOS* CLINIC ANOPHTHALMOS NOS CONGEN CYSTIC EYEBALL CRYPTOPHTHALMOS MICROPHTHALMOS* MICROPHTHALMOS NOS SIMPLE MICROPHTHALMOS MICROPHTH W OTH EYE ANOM BUPHTHALMOS* BUPHTHALMOS NOS SIMPLE BUPHTHALMOS BUPHTHAL W OTH EYE ANOM CONG CATARACT/LENS ANOM* CONGENITAL CATARACT NOS CAPSULAR CATARACT CORTICAL/ZONULAR CATARAC NUCLEAR CATARACT CONG TOT/SUBTOT CATARACT CONGENITAL APHAKIA ANOMALIES OF LENS SHAPE CONGENITAL ECTOPIC LENS CONG CATAR/LENS ANOM NEC ANTERIOR SEGMNT ANOM NEC* ANOM CORNEAL SIZE/SHAPE CONG CORNEA OPAC AFF VIS CONG CORNEAL OPACIT NEC ANOM ANTER CHAMBER-EYE ANIRIDIA ANOMALIES OF SCLERA MULT ANOM ANTER SEG-EYE ANOM ANTER SEG NEC-EYE CONG ANOM POST SEG-EYE* VITREOUS ANOMALIES FUNDUS COLOBOMA CONG CHORIORETINAL DEGEN CONG FOLD/CYST POST EYE CONG MACULAR CHANGE-EYE

77. Alphabetical Topic Index (AZ) Jump To A B C D E F G H I J K L M Ankylosing Spondylitis Spondylitis, Ankylosing Anodontia (Absence of Teeth) AnodontiaAnomia (Difficulty Talking) Anomia anophthalmos anophthalmos Anovulation http://www.uscuh.com/apps/Intermap/topiclist/SectionA.html

Alphabetical Topic Index (A-Z): Jump To: A B C D ... Ax A Ab Abdominal Cancer Seeding Neoplasm Seeding Abdominal Problems Colorectal Cancer Overview Early Stage Colorectal Cancer Stage I Colorectal Cancer Liver Cirrhosis ... Stage II or III Colorectal Cancer Abducens Nerve Injury Abducens Nerve Injury Abetalipoproteinemia Abetalipoproteinemia Abnormal Menstrual Bleeding Abnormal Menstrual Bleeding Abnormal Pap/Dysplasia Abnormal PAP Smear Cervical Dysplasia Abortion, Incomplete Abortion, Incomplete Abortion, Missed Abortion, Missed Abortion, Septic Abortion, Septic Abortion, Threatened Abortion, Threatened Abuse - Physical or Mental Rape Shaken Baby Syndrome Back To Top ^ Ac Acanthamoeba Keratitis Acanthamoeba Keratitis Acantholysis Acantholysis Acanthosis Nigricans Acanthosis Nigricans Acatalasia Acatalasia Accelerated Idioventricular Rhythm Accelerated Idioventricular Rhythm Accessory Nerve Diseases Accessory Nerve Diseases Achlorhydria Achlorhydria Achondroplasia Achondroplasia Acinetobacter Infections Acinetobacter Infections Acne Acne Overview And Treatment Acne Keloid Acne Keloid Acoustic Neuroma Neuroma, Acoustic

78. Rare Diseases List - Office Of Rare Diseases Anophthalmia short stature obesity. Anophthalmia Waardenburg syndrome. anophthalmoswith limb anomalies. anophthalmos, clinical. Anorchia. Anorchidism. http://ord.aspensys.com/diseases.asp

Office of Rare Diseases Rare Diseases List An orphan or rare disease is generally considered to have a prevalence of less than 200,000 affected individuals in the USA. Certain diseases with more than 200,000 affected individuals are included but subpopulations of these conditions may be less than the prevalence standard for rare disease. This list includes rare diseases and conditions for which information requests have been made to the Office of Rare Diseases. It is updated on a regular basis. We welcome suggestions for additions to the list and your recommendations may be sent via email to: ord@od.nih.gov Please Note: The names of the conditions (listed in alphabetical order) may not necessarily be the most frequently used ones. Clicking on one of the names below will take you to a page that contains information specific for that disease. The links on that page will take you to several sources of information, including: ClinicalTrials.gov, an NIH site that lists ongoing clinical trials; Online Mendelian Inheritance in Man (OMIM), an NIH site authored and edited by Johns Hopkins University, with information on specific genetic diseases; and

79. RACHEL's Environment And Health Weekly #410 Microcephalus (small head), 2.12, 2.61, 3.0%. EYES. anophthalmos (absence of eyes),0.57, 0.68, 2.6%. Congenital cataract (eye cataracts at birth), 0.71, 1.02, 5.3%. http://www.ejnet.org/rachel/rehw410.htm

=======================Electronic Edition======================== -October 6, 1994- News and resources for environmental justice. Environmental Research Foundation P.O. Box 5036, Annapolis, MD 21403 Fax (410) 263-8944; Internet: erf@igc.apc.org The Back issues and Index are available here. The official RACHEL archive is here. It's updated constantly. To subscribe , send E-mail to rachel- weekly-request@world.std.com with the single word SUBSCRIBE in the message. It's free. Previous Issue Next Issue BIRTH DEFECTS PART 1 The Birth Defects Monitoring Program (BDMP) is a U.S. government effort to monitor birth defects (congenital malformations) using data collected when newborn infants are discharged from the hospital. The BDMP was initiated by the federal Centers for Disease Control (CDC) in 1974. The current BDMP database includes information on roughly 15 million births that have occurred at 1200 predominantly mid-sized community hospitals in the U.S. during the past 20 years. The BDMP database is not comprehensive (it does not include information on every birth that occurs in the U.S.). Neither does it represent a randomly-selected sample of all U.S. births; therefore data from the BDMP cannot be considered representative of the entire "universe" of all U.S. newborns. In 1987 the BDMP received information on 15% of all U.S. births, which gives an idea of how comprehensive the coverage is. Because the data are mostly from mid-sized hospitals, we might expect that some of the largest hospitals in the largest cities are under-represented. Nevertheless, as the CDC says, the BDMP "represents the largest single set of uniformly collected and coded discharge data on congenital malformations in the United States." It is simply the best information available on birth defects in the U.S.

80. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE Anomia. ANOPHTHALMIA anophthalmos ABSENCE of EYE TISSUE. Search PUBMEDfor articles on anophthalmos All Review Therapy Diagnosis. ANORCHIE http://www.vada.nl/medisch/medani.htm

VADA - GEZONDHEID en ZIEKTE HEALTH and DISEASE ANI - ANZ OPGELET - ATTENTION Patienten en leken die raadgevingen/adviezen/informatie zoeken via deze verzameling links wordt dringend geadviseerd de verzamelde informatie te bespreken met de (behandelend) arts/specialist/hulpverlener. Patients and lay persons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. ANIMAL ASSISTED THERAPY Therapet Animal Assisted Therapy Foundation Animal Assisted Therapy Homepage for proponents of this practice proven to increase physiological and psychological recovery rate of patients ANIMAL SALMONELLA INFECTIONS See also: See also: GRAM-NEGATIVE BACTERIAL INFECTIONS See also: ENTEROBACTERIACEAE INFECTIONS See also: BACTERIAL INFECTIONS and MUCOSES See also: SALMONELLA INFECTIE Search PUBMED for articles on Salmonella Infections, Animal: All Review Therapy Diagnosis ANIRIDIA See also: OOGAANDOENINGEN EYE DISEASES See also: OOGAFWIJKINGEN EYE ABNORMALITIES See also: WAGR SYNDROOM WAGR SYNDROME See also: GILLESPIE SYNDROOM GILLESPIE SYNDROME Med. Coll. of Wisconsin:Aniridia

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