1Up Health > Health Links Directory > Conditions And Diseases: M Atrophic Papulosis (4) Malnutrition (9) Mannosidosis (2) Marburg (6) Marfan Syndrome(40) MarieSainton Disease (6) marinesco-sjogren syndrome (5) Mayer http://www.1uphealth.com/links/conditions-and-diseases-m.html
Extractions: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites. Home Contact Us Privacy Links Directory
Searchalot Directory For M Syndrome (39); MarieSainton Disease (6); marinesco-sjogren syndrome(5); Mayer Rokitansky Kuster Hauser Syndrome (10); McArdle's Disease http://www.searchalot.com/Top/Health/ConditionsandDiseases/M/
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GS MAPLE SYRUP URINE DISEASE, TYPE IB(OMIM) MARDENWALKER SYNDROME(OMIM) marinesco-sjogren syndrome; MSS(OMIM http://nigiwai.net/gs1/omim8.htm
The Kuwait Medical Genetics Centre entity of syndromic dextrocardia, cases of Joubert's syndrome, SmithLemli-Opitzsyndrome, Sjogren-Larsen syndrome, marinesco-sjogren syndrome, Troyer- like http://www.safat.com/kgc.html
Extractions: The accurate diagnosis of rare monogenic diseases. Investigating cases of congenital malformations. Providing genetic counselling for families with genetic disorders e.g. cases of male/female primary infertility, recurrent pregnancy loss, congenital malformations, structural/numerical chromosomal abnormalities, genetic forms of mental retardation, f amilial visual disorders and pre-marital counselling. Exploring the possible means of reducing neonatal mortality and physical disability. Providing training programmes for doctors and technical staff in the area of genetic counselling. The KMGC represents an independent entity located in the Maternity Hospital, and is affiliated to the Ministry of Health. The service is provided to a population size of 1.575.983 persons, including 655.820 (41.6%) Kuwaiti citizens and 920.163 (58.4%) non -Kuwaiti residents, mostly of Arab nationalities. The service is provided in liaison with departments of different specialities in satellite Genetics clinics attached to 5 regional hospitals including: Sabah and Ameri Hospital (serving 192.800 persons)
Rare Disease Support Community Syndrome Type I Marfan Syndrome Type II Marfan Syndrome Type III Marfan SyndromeType IV Marfan Syndrome Type V marinescosjogren syndrome Maroteaux-Lamy http://www.angelfire.com/on2/egroups/M
Extractions: Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Eye Cataract - close-up of the eye Rubella Syndrome Cataract Alternative names Return to top Cataract - congenital Definition Return to top A cataract is any clouding of the lens of the eye. a congenital cataract is an opacity of the lens that occurs in the fetus at some time during pregnancy and is present at birth. Causes, incidence, and risk factors Return to top Although there are many diseases and inherited disorders that can lead to congenital cataracts, the actual incidence of congenital cataracts is low. In most patients with congenital cataract, no specific cause can be identified.
Select Entries From OMIM -- Online Mendelian Inheritance In Man 123580 CRYSTALLIN, ALPHAA; CRYAA *120140 COLLAGEN, TYPE II, ALPHA-1; COL2A1 *261600PHENYLKETONURIA *248800 marinesco-sjogren syndrome; MSS *115650 CATARACT http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/eye/congen_cataract.htm
UNSW Embryology-OMIM Scoliosis List 271270 SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM *300061 MENTAL RETARDATION, XLINKED;DXS6673E *248800 marinesco-sjogren syndrome; MSS *249310 MEGALOCORNEA http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/skmus/OMIM-scoliosis_list.htm
Extractions: MUSCULOSKELETAL DEVELOPMENT Embryology Home Page Select Entries from OMIM Online Mendelian Inheritance in Man (Internet Link) This page is for computers without external internet access. Internet access computers can see the full description of the abnormality from the links below. Back to UNSW Embryology-Musculoskeletal Notes 160 entries found, searching for " scoliosis SCOLIOSIS, IDIOPATHIC
NIH Guide: THE HEREDITARY ATAXIAS INCLUDING MACHADO-JOSEPH DISEASE hereditary cerebellar ataxias, ataxiatelangiectasia, hereditary spastic paraplegia,Roussy-Levy and marinesco-sjogren syndrome, abetalipoproteinemia (Bassen http://grants.nih.gov/grants/guide/pa-files/PA-92-048.html
Browsing Health Conditions And Diseases M Category Syndrome Malignant Atrophic Papulosis Malnutrition Mannosidosis Marburg MarfanSyndrome MarieSainton Disease marinesco-sjogren syndrome Mayer Rokitansky http://www.uksprite.com/search/search/Health/Conditions_and_Diseases/M/
Useful Links March of Dimes Birth Defects Foundation, Marfan Syndrome National MarfanFoundation, 3285. marinescosjogren syndrome Support Website, 3438. http://www.possum.net.au/links.htm
Extractions: Upcoming release - web enabled POSSUM read more... About Find out about the latest version of POSSUM. FAQ Frequently Asked Questions about POSSUM. Order Print an order form and send it to us. Links Discover syndrome web sites using our new list of useful links. Contact Maybe you'd like to tell us what you think about POSSUM, contribute pictures to the POSSUM database, or make some suggestions about how we can improve this website. Useful Links The information listed below is provided for informational purposes only. There is no implied endorsement by POSSUM. POSSUM does not promote or endorse participation in any specific organization. Every effort is made to ensure that the details for each entry are as current as possible. Syndrome Name POSSUM Number Aarskog Syndrome Parents Support Group (USA) Aarskog Syndrome Parents Support Group (UK) Aicardi Syndrome Foundation Alagille Syndrome Alliance ... WAGR/Aniridia Network
Health Library - Marinesco Sjogren Syndrome Search. Marinesco Sjogren Syndrome. None. General Discussion. marinescosjogren syndromeis a rare disorder that is inherited through autosomal recessive genes. http://yourhealth.stlukesonline.org/Library/HealthGuide/IllnessConditions/topic.
Extractions: hair defects table Home Forums Privacy Advertising ... Home On this page... Introduction The tables below records disorders known to involve hair shaft defects. The first table lists disorders where hair defects are a primary symptom. The second table lists disorders where hair defects can be one of several symptoms. Typically the other symptoms are of greater concern and health/life threatening. Links to relevant web pages on the Online Mendelian Inheritance in Man (OMIM) web database are also given where possible. Where a disorder is known by more than one name, alternative names are given in the second column and the record duplicated in the first column under each respective name. Brackets around alternative disorder names indicate an indirect association, for example a subcategory of the disorder. These records are not duplicated in the first column. List of disorders involving hair fiber defects as a primary symptom Disorders with hair defects as a primary symptom Alternative names for disorder Links to OMIM web pages for disorder (where available) Allotrichia circumscripta symmetrica capillitii
Extractions: hypotrichosis table Home Forums Privacy Advertising ... Home On this page... Introduction The tables below records disorders known to involve hypotrichosis. The first table lists disorders where hypotrichosis is a primary symptom. The second table lists disorders where hypotrichosis can be one of several symptoms. Typically the other symptoms are of greater concern and health or life threatening. Many of these conditions involving hypotrichosis as a secondary symptom are ectodermal dysplasias. The clinical distinction between alopecia and hypotrichosis is that alopecia involves hair growth that is later lost. Hypotrichosis is a lack of any hair growth. The distinction between alopecia and hypotrichosis is not clear cut for many disorders. Some dermatologists will disagree with my listing. You may find some disorders in both the alopecia and hypotrichosis listings. This is not necessarily a complete list of disorders involving hypotrichosis. Links to relevant web pages on the Online Mendelian Inheritance in Man (OMIM) web database are also given where possible.
1992 KJMS TI marinescosjogren syndrome with reduced cytochrome c oxidase in muscle.AU Kodama-S; Komatsu-M; Miyoshi-M; Nakao-H; Sakurai-T; UM. http://www.med.kobe-u.ac.jp/journal/contents/1992/245-54(1992).html
AtaxiasUntitled and eunuchoidism), Hereditary ataxia (with myotonia and cataracts), Hypertrophicinterstitial neuritis, marinescosjogren syndrome, Pelizaeus-Merzbacher disease http://www.cmdg.org/Movement_/ataxias/ataxias.htm
Extractions: The Canadian Movement Disorder Group Ataxia Ataxia is a term to describe loss of balance. The part of the brain that is involved in balance is at the back of the brain, attached to the brainstem, and is called the "Cerebellum". Damage to the cerebellum or its connections will result in unsteadiness of walking, and clumsiness of hand and foot coordination. Many conditions can cause the cerebellum to stop working normally. Cause of Ataxia include a huge number of conditions: Drug / Toxin induced cerebellar dysfunction: These include drugs; Clonazepam, Tegretol, Phenobarb, Primidone, Dilantin and toxins including; acute alcohol intoxication, alcoholism, solvent abuse , lead / mercury Trauma to the cerebellum Head Injury Endocrine Disorders (diseases of the glands that release hormones) Hypothyroidism Nutritional Deficiencies Vitamin B12 deficiency Neoplastic (Tumor) Paraneoplastic (Associated with a distant tumor) Vascular Causes (Stroke) These include; vasculitis (inflamation of blood vessels eg. Lupus), angioblastoma (a tumor of the blood vessels), embolism (a blood clot plugging a blood vessel), hemorrhage (a blood vessel rupturing and bleeding into the cerebellum), and Von-Hippel-Lindau Syndrome (a disorder of blood vessel formation)
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