41. SpringerLink: Archives Of Gynecology And Obstetrics - Abstract Volume 265 Issue 157. case report silverrussell syndrome associated to Mayer-Rokitansky-Kuster-Hausersyndrome, diabetes and hirsutism. J. Bellver http://link.springer-ny.com/link/service/journals/00404/bibs/1265003/12650155.ht

Archives of Gynecology and Obstetrics ISSN: 0932-0067 (printed version) ISSN: 1432-0711 (electronic version) Table of Contents Abstract Volume 265 Issue 3 (2001) pp 155-157 case report : Silver-Russell syndrome associated to Mayer-Rokitansky-Kuster-Hauser syndrome, diabetes and hirsutism (1) Department of Gynecologycal Endocrinology, Hospital Universitario ''La Fe'', Calle Regacho, 8-14, Mislata 46920, Valencia, Spain e-mail: jbellverp@sego.es. Tel.: 011-34-963624399, Fax: 011-34-963694735 (2) Department of P.O.G. Faculty of Medicine, University of Valencia, Spain (3) Department of Gynecology, Hospital Universitario ''La Fe'', Valencia, Spain Received: 4 December 2000 / Accepted: 31 January 2001 Abstract Keywords Article in PDF format (44 KB) Online publication: August 2, 2001 SpringerLink Helpdesk

42. Publikationen Der Abteilung Medizinische Genetik Tübingen Kaiser P, Ranke MB, Eggermann T(1999) Biparental Expression of IGFBP1 and IGFBP3renders their Involvement in the Etiology of silverrussell syndrome unlikely. http://www.uni-tuebingen.de/Klinische_Genetik/publ_1999.html

Publikationen Autoren, Daten und Titel Eggermann K, Wollmann HA, Tomiuk J, Ranke MB, Kaiser P Eggermann T Screening for mutations in the promotor and the coding region of the IGFBP1 and IGFBP3 genes in SRS patients. Hum Hered 49:123-128 Albers A , Lahme S, Waldegger S, Kaiser P , Zerres K, Capasso G, PIca A, Lang F, Eggermann T Mutations in the SLC3A1 gene in unselected cystinuric patients. Genetic Testing: 3:227-232 Eggermann K , Wollmann HA, Binder G, Kaiser P , Ranke MB, Eggermann T Biparental Expression of IGFBP1 and IGFBP3 renders their Involvement in the Etiology of Silver-Russell Syndrome unlikely. Albers A Kaiser P Eggermann T , Wagner C, Lang F Identification of mutations in the SLC3A1/rBAT gene causing cystinuria and functional characterization fo two mutations. Albers A Kaiser P , Bichler KH, Lang F, Zerres K Eggermann T Identification of mutations in the SLC3A1 gene in cystinuric patients and functional characterization of 5 mutations. Eur J Hum Genet 7S:P-413 Mergenthaler S , Blagitko N, Schulz U, Ropers HH, Kaiser P , Ranke MB,Wollmann HA, Kalscheur V, Eggermann T Molecular genetic investigation on GRB10.

43. Dwarfism Types And Definitions silverrussell syndrome Silver syndrome. See Russell-Silver syndrome.Spherophakia-brachymorphia syndrome. See Weill-Marchesani syndrome. http://www.lpaonline.org/resources_dwarftypes.html

LPA Online Dwarfism Resources TYPES AND DEFINITIONS This page is not intended as a complete guide to the different types of dwarfism. After all, there are an estimated 200 types, some of which have never even been named. Nor is this page meant to be the last word. Think of this page as a starting point as you begin to learn about your child's condition. In addition to this page, you may want to check Dwarfism.org's "Types of Dwarfism" section, a compilation of 875 names of dwarfism and dysplasia types. The conditions are linked to genetic descriptions at the Online Mendelian Inheritance in Man (OMIM), a project of the National Center for Biotechnology Information. OMIM entries are quite technical far more so than the information and links you'll find here but is the only online information available for many types of genetic conditions. Information about other types of dwarfism, and additional resources for those already listed, are always welcome. Send them to the LPA Online webmaster, Dan Kennedy, at

44. •¶Œ£ˆê—— Kishino T, Tanaka T, Yamada M, Tsutsumi O, Niikawa N, KanekoIshino T, Ishino F.No evidence of PEG1/MEST gene mutations in silver-russell syndrome patients. http://www.ishino.bio.titech.ac.jp/list.html

•¶Œ£ƒŠƒXƒg Lee J, Inoue K, Ono R, Ogonuki N, Kohda T, Kaneko-Ishino T, Ogura A, Ishino F. Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells. Development. 2002 Apr 15;129(8):1807-1817. Inoue K, Kohda T, Lee J, Ogonuki N, Mochida K, Noguchi Y, Tanemura K, Kaneko-Ishino T, Ishino F, Ogura A. Faithful expression of imprinted genes in cloned mice. Science. 2002 Jan 11;295(5553):297. Kobayashi S, Kohda T, Ichikawa H, Ogura A, Ohki M, Kaneko-Ishino T, Ishino F. Paternal expression of a novel imprinted gene, , in the mouse 7C region homologous to the Prader-Willi syndrome region. Biochem Biophys Res Commun. 2002 Jan 11;290(1):403-408. Kobayashi S, Uemura H, Kohda T, Nagai T, Chinen Y, Naritomi K, Kinoshita EI, Ohashi H, Imaizumi K, Tsukahara M, Sugio Y, Tonoki H, Kishino T, Tanaka T, Yamada M, Tsutsumi O, Niikawa N, Kaneko-Ishino T, Ishino F. No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients. Am J Med Genet. 2001 Dec 1;104(3):225-231. Ono R, Kobayashi S, Wagatsuma H, Aisaka K, Kohda T, Kaneko-Ishino T, Ishino F.

45. UK Self Help Groups: S 8961 7795. silverrussell syndrome. contact silver-russell syndromeSupport Group c/o CaF, Tel 020 7383 3555. Single Parents. Care for http://www.ukselfhelp.info/s.htm

Main Index IMPORTANT - Please use www.ukindex.info and/or the links at the foot of this page to help maintain this free resource. Click directly on the name of the condition below to reveal the associated group(s). Sacral Agenesis Sacral Agenesis Support Group, Tel 023 8084 2661 SADS (Sudden Adult Death Syndrome) contact SADS UK , Tel 01277 230 642 Sadistic Abuse/Satanic Abuse SAFE (Supporting Survivors of Sadistic Abuse), Tel 01722 410889 Saethre-Chotzen Syndrome contact Craniofacial Support Group , Tel 01926 334 629 Saggital Synostosis contact Craniofacial Support Group , Tel 01926 334 629 Salaam Seizures contact West Syndrome Support Group , Tel 020 8680 8449 Sanfillipo Syndrome contact Society for Mucopolysaccharide Diseases , Tel 01494 434 156 Sarcoidosis contact SILA (Sarcoidosis and Interstitial Lung Association) , Tel 020 7237 5912 Scabies contact CHC (Community Hygiene Concern), Tel 020 7686 4321 Scheie Syndrome contact Society for Mucopolysaccharide Diseases , Tel 01494 434 156 Schilder's Disease contact Adrenoleukodystrophy Support , Tel 020 7631 3336 Scheurmann Disease contact Perthes Association , Tel 01483 306 637 Schizophrenia National Schizophrenia Fellowship , Tel 020 8547 3937 Schizophrenia Association of Great Britain , Tel 01248 354 048 School Phobia contact Parentline Plus , Tel 020 7284 5500 see under bullying if this is the cause of the phobia Scleroderma

46. Newsletter References Ranke MB, Lindberg A. Growth hormone treatment of short children born small forgestational age or with silverrussell syndrome results from KIGS (Kabi http://www.aap.org/sections/Endocrinology/references.htm

Members Only Channel Search Site Map BookStore ... Home References from Summer/Fall Newsletter GROWTH HORMONE SHOULD NOT BE ADMINISTERED ROUTINELY TO CHILDREN WITH SHORT STATURE DUE TO INTRAUTERINE GROWTH RETARDATION WHO ARE NOT CLASSICALLY GROWTH HORMONE DEFICIENT Allen W. Root, MD Departments of Pediatrics, Biochemistry and Molecular Biology, University of South Florida College of Medicine, Tampa, FL All Children's Hospital, St. Petersburg, Florida References Botero D, Lifshitz F. Intrauterine growth retardation and long-term effects on growth. Curr Opin Pediatr 11:340-347,1999. Chatelain P, Peretti N, Lapillonne A, Nicolino M, Salle B, et al. New insights into the postnatal growth of infants born "idiopathic' small for gestational age. J Pediatr Endocrinol Metab 14:1515-1519,2001. Coutant R, Carel J-C, Letrait M, Bouvattier C, Chatelain P, Coste J, Chaussain J-L. Short stature associated with intrauterine growth retardation: Final height of untreated and growth hormone-treated children. J Clin Endocrinol Metab 83:1070-1074,1998. de Zegher F. Growth hormone treatment in intrauterine growth retardation. 84th Annual Meeting of the Endocrine Society, San Francisco, CA, June 19-22, 2002, Abst S8-1, p 26.

47. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE SYNDROOM van SILVERRUSSELL silver-russell syndrome RUSSELL-SILVERSYNDROME RUSSELL SYNDROME SILVER SYNDROME RSS. Russell-Silver http://www.vada.nl/medisch/medsim.htm

VADA - GEZONDHEID en ZIEKTE HEALTH and DISEASE SI - SM 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. SIALIDOSE SIALIDOSIS See also: LYSOSOMEN See also: GALACTSIALIDOSE GALACTSIALIDOSIS Sialidosis and Galactosialidosis SIALORRHOE HYPERSALVATIE SIALORRHEA See also: SPEEKSEL SALIVA Sialorrhea SICK BUILDING SYNDROME See also: ALLERGIE ALLERGY Centrum Gezondheidsbevordering op de Werkplek, den Haag Sick Building Syndrome Introduction to this recently identified condition, its causes, effects, and solutions See also: DIKKE DARM COLON ASCENDING COLON TRANSVERSE COLON DESCENDING COLON SIGMOID COLON See also: ENDOSCOPIE ENDOSCOPY See also: ANOSCOPIE ANOSCOPY See also: COLOSCOPIE COLOSCOPY See also: PROCTOSCOPIE PROCTOSCOPY See also: COLONOSCOPIE COLONOSCOPY Sigmoidoscopie (endoscopie van de binnenbekleding van de laatste 50 – 60 centimeter van de dikke darm) Darmkanker: Preventiefonderzoek voor risicodragers Flexible Sigmoidoscopy SIKKELCELZIEKTE SCZ SIKKELCELBLOEDARMOEDE SICKLE CELL DISEASE SICKLE CELL ANEMIA See also: BLOEDARMOEDE ANEMIE ANEMIA Organisatie Sikkel Cel Anemie Research Holland (OSCAR), Telefoon: 020-6797887

48. Themen Für DoktorarbeitenInstitut Für Anthropologie Und Humangenetik, Abteilun Translate this page Wollmann HA, Kirchner T, Enders H, Preece MA, Ranke MB (1995) Growth and symptomsin silver-russell syndrome review on the basis of 386 patients. http://nero.anatom.uni-tuebingen.de/gk/anlage1_6.html

Teilnehmer am Kolleg: Prof. Dr.med. P. Kaiser Forschungsgebiet: Klinische Genetik Methoden: Zellkulturen, cytogenetische Methoden, Molekulargenetische Methoden Sekretariat: 07071-29-76404 (Tel.), 07071-296406(Fax) Methoden: A Cytogenetik Zellkultur Lymphozyten, Amnionzellen, Gewebe Chromosomenanalyse FISH 1. Chromosomen-Painting 2. Interphase-FISH 3. Mikrodeletionen B Molekulargenetik Arbeitsschwerpunkte: A Patientenversorgung Genetische Beratung Dr. H. Enders (Tel. -72190) Dr. U. Mau/Dr. A. Dufke (Tel.-76405) Zur Syndromzuordnung Zur Familienplanung Cytogenetische Diagnostik Dr. C. Backsch/ Dipl.-Biol. U. Heinrich (Tel. -72191) Dr. U. Klein-Vogler (Tel. -76163) Postnatale Chromosomenanalyse Molekulargenet. Diagnostik Dr. T. Eggermann/Dipl.-Biol. K. Eggermann (Tel. -75431) Cystische Fibrose Fragiles X-Syndrom Uniparentale Disomien Chromosomenaberrationen B Forschungsschwerpunkte Allgemeine Cytogenetik (Backsch/Heinrich) Pericentrische Inversionen, Interphasediagnostik, FISH Molekulargenetik (Eggermann/Eggermann) Herkunftsstudien zu Chromosomenaberrationen Silver-Russell-Syndrom Cystinurie Promotionen der letzten 3 Jahre Laufende Dissertationen: Maier, C.: Die Anwendung der in-situ-Hybridisierung zur Diagnostik gonosomaler Chromosomenaberrationen.

49. ËÁÍà´ç¡µÍº RussellSilver Syndrome (RSS) silver-russell syndrome, Silver Syndrome ? Russell Syndrome. http://www.doolaedek.com/Consult/Doolae_Ans.asp?Q=1679

50. Max Planck Weekly Research Report - Human Biology/Medical Research Human Genetics. 6(2)114120, 1998 Mar-Apr. Author Keywords Peg1/mest,silver-russell syndrome, Uniparental disomy, Imprinting. http://www.reports.mpg.de/1998/24/199824_h.htm

Biologisch-Medizinische Forschung Biological and Medical Sciences Humanbiologie/Medizin Human Biology/Medical Research Citation No. 9824-15 (ISI acc.no.ZP144-0005) Authors Barten R, Meyer TF. Title CLONING AND CHARACTERISATION OF THE NEISSERIA GONORRHOEAE AROB GENE Source Author Keywords 3-dehydroquinate synthetase, Aromatic amino acid synthesis, Arok, Yafj. Cell invasion. KeyWords Plus by ISI Dependent salmonella-typhimurium, Amino-acid sequence, Escherichia-coli. Epithelial-cells, Chromosomal rearrangement, Shuttle mutagenesis, Phase variation, Dna-sequence, Protein, Construction. Abstract Publication Type Article CC Categories Institution Reprint available from: Meyer TF MAX PLANCK INST BIOL INFEKT BIOL ABT SPEMANNSTR 34 D-72076 TUBINGEN GERMANY MAX PLANCK INST BIOL INFEKT BIOL ABT D-72076 TUBINGEN GERMANY MAX PLANCK INST INFEKT BIOL D-10117 BERLIN GERMANY Citation No. 9824-32 (ISI acc.no.ZP033-0029) Authors Hoffrage U, Gigerenzer G. Title USING NATURAL FREQUENCIES TO IMPROVE DIAGNOSTIC INFERENCES Source Academic Medicine. 73(5):538-540, 1998 May.

51. Max Planck Weekly Research Report - Human Biology/Medical Research VM, Wollmann HA, Eggermann T. Author email Address teggermann@post.klinikum.rwth-aachen.deTitle Gene dosage analysis in silver-russell syndrome Use of http://www.reports.mpg.de/2002/05/200205_h.htm

Biologisch-Medizinische Forschung Biological and Medical Sciences Humanbiologie/Medizin Human Biology/Medical Research Citation No. 200205-57 (ISI acc.no.510EY-0008) Document Delivery Citation No. 200205-57 (ISI acc.no.510EY: Document Delivery available) Authors Fischer S, Wobben M, Marti HH, Renz D, Schaper W. Title Hypoxia-induced hyperpermeability in brain microvessel endothelial cells involves VEGF-mediated changes in the expression of zonula occludens-1 Source Microvascular Research. 63(1):70-80, 2002 Jan. Abbreviated Source Microvasc. Res. 63(1):70-80, 2002 Jan. ACADEMIC PRESS INC, 525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA. URL: http://www.apnet.com ISSN Author Keywords Hypoxia, Endothelial cells, Hyperpermeability, Vegf (vascular endothelial growth factor), Zonula occludens-1. KeyWords Plus by ISI Vascular-permeability factor, Tumor-suppressor protein, Growth-factor, Tight junctions, Zo-1, Occludin, Porcine, Actin, Identification, Angiogenesis. Abstract Language English Publication Type Article Subset Current Contents(R)/Life Sciences.

52. Full Listing SHINGLES AND PHN, SHPRINTZEN SYNDROME, SHWACHMAN SYNDROME, SIALIC ACID STORAGEDISEASE, SIALIDOSIS, SICKLE CELL, silverrussell syndrome, SINGLE PARENTS http://www.doctor.gp/help/full_listing.htm

DIRECTORY OF BRITISH SELF HELP GROUPS AND SUPPORT ORGANISATIONS by Steve and Julie Garrill Home

53. Medizinische Genetik Martinez MJ, Binkert F, Schinzel A, Kotzot D. No Evidence of dup(7)(p11.2p13) insilverrussell syndrome Am J Med Genet 2001 99; 335-337 Schinzel A, Niedrist D http://www.medgen.unizh.ch/Pages/Pub.html

Angelman Syndrom Beckwith-Wiedemann Syndrom CATCH-22 Chromosomenuntersuchung cystische Fibrose FISH-Schnelltest fragiles X Syndrom Klinefelter Syndrom Myotone Dystrophie Steinert Prader-Willi Syndrom Rett Syndrom Silver-Russel Syndrom (UPD7) Subtelomer-FISH Turner Syndrom Williams Syndrom - Zytogenetik - Molekulargenetik Albright Syndrom Angelman Syndrom Bardet-Biedl Syndrom Beckwith-Wiedemann Syndrom CATCH-22 Cystische Fibrose Chorea Huntington Fragiles X Syndrom Miller-Dieker Syndrom Myotone Dystrophie Steinert Neuralrohrdefekte Neurofibromatose Prader-Willi Syndrom Rett Syndrom Spinale Muskelatrophie Smith-Magenis Syndrom Uniparentale Disomie Williams Syndrom Martinez M-J, Binkert F, Schinzel A, Kotzot D. No Evidence of dup(7)(p11.2p13) in Silver-Russell Syndrome Am J Med Genet 2001 99; 335-337 Schinzel A, Niedrist D. Chromosome Imbalances Associated With Epilepsy Am J Med Genet (Semin. Med. Genet.) 2001 106; 119-124 Weymann S, Yonekawa Y, Khan N, Martin E, Heppner F L, Schinzel A, Kotzot D. Severe Arterial Occlusive Disorder and Brachysyndactyly in a Boy: A Further Case of Grange Syndrome? Am J Med Genet 2001 99; 190-195

54. Medizinische Genetik Translate this page Ropers HH, Kalscheuer VM. Evidence against a major role of PEG1/MESTin silver-russell syndrome. Eur J hum Genet (1998) 6, 114-120. http://www.medgen.unizh.ch/Pages/Pub98.html

Angelman Syndrom Beckwith-Wiedemann Syndrom CATCH-22 Chromosomenuntersuchung cystische Fibrose FISH-Schnelltest fragiles X Syndrom Klinefelter Syndrom Myotone Dystrophie Steinert Prader-Willi Syndrom Rett Syndrom Silver-Russel Syndrom (UPD7) Subtelomer-FISH Turner Syndrom Williams Syndrom - Zytogenetik - Molekulargenetik Albright Syndrom Angelman Syndrom Bardet-Biedl Syndrom Beckwith-Wiedemann Syndrom CATCH-22 Cystische Fibrose Chorea Huntington Miller-Dieker Syndrom Myotone Dystrophie Steinert Neuralrohrdefekte Neurofibromatose Prader-Willi Syndrom Rett Syndrom Spinale Muskelatrophie Smith-Magenis Syndrom Uniparentale Disomie Williams Syndrom 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin. Clin Genet 1998;53:63-69 Robinson WP, Dutly F, Nicholls RD, Bernasconi F, Penaherrera M, Michaelis RC, Abeliovich D, Schinzel AA. The mechanisms involved in formation of deletions and duplications of 15q11-q13. J Med Genet 1998; 35: 130-136 Dutly F, Balmer D, Baumer A, Binkert F, Schinzel A. Isochromosomes 12q und 9p: parental origin and possible mechanisms of formation.

55. UCL Division Of Paediatric And Adolescent Endocrinology 10% of patients with silverrussell syndrome have maternal uniparental disomy ofchromosome 7 which implies that maternally imprinted genes are involved with http://www.ucl.ac.uk/medicine/endocrinology/res.html

Division of Paediatric and Adolescent Endocrinology Synopsis of Current Research a) Developmental Endocrinology and Growth Regulation Molecular embryology of somatotroph function in the human anterior pituitary focussing on the identification of the cause of congenital panhypopituitarism. We have described the cascade of homeobox genes in the condition of septo-optic dysplasia (SOD) in man, a (relatively) common cause of congenital panhypopituitarism in our clinic Identification of the imprinted gene(s) on human chromosome 7 responsible for intrauterine growth retardation and the role of the insulin-life growth factor axis in this syndrome. 10% of patients with Silver-Russell syndrome have maternal uniparental disomy of chromosome 7 which implies that maternally imprinted genes are involved with the SRS phenotype. Four candidate genes have been identified and are now being studied in detail. There is evidence from samples taken by cordocentesis and at birth of perturbatons in the IGF axis in IUGR but the mechanisms and effects are unclear. The role of the DAX-1 gene in the development of the adrenal cortex and of gonadotrophin-releasing hormone (GnRH).

56. S ShyDrager Syndrome; @ Sickle Cell Disease; @ silver-russell syndrome;@ Sinusitis; @ Sitosterolemia; @ Skin Disorders; @ Sleep Apnea; http://www.ad.com/Health/Conditions_and_Diseases/S/

search Top Categories: SIDS @ Sagittal Synostosis @ Salmonellosis @ San Joaquin Valley Fever ... @ Systemic Lupus Erythematosus AD.COM Web Directory is based on ODP - Open Directory Project data. No proprietary software was used in the development of this web site. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor

57. Error Page Translate this page MALADIE silver-russell, syndrome de, CIM Q87.17, Le syndrome desilver-russell associe un retard de croissance débutant pendant http://orphanet.infobiogen.fr/Site/Exp.stm?Lng=FR&Expert=813

58. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE See also RHIZOMELIC CHONDRODYSPLASIA PUNCTATA See also RUSSELLSILVER syndromeSee also SYNDROOM van silver-russell SILVER- RUSSELL syndrome See also http://www.vada.nl/medisch/meddvz.htm

VADA - GEZONDHEID en ZIEKTE HEALTH and DISEASE DV - DZ 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. DWANGMATIG EETGEDRAG ANONIEME OVERETERS ANONYMOUS OVEREATERS See also: EETSTOORNISSEN EATING DISORDERS Overeaters Anonymous - Anonieme Overeters Dwangmatig eetgedrag DWANGSTOORNIS DWANGNEUROSE OBSESSIEF-COMPULSIEVE STOORNISSEN OBSESSIVE-COMPULSIVE DISORDER OCD See also: ANGSTSTOORNISSEN See also: TRICHOTILLOMANIE TRICHOTILLOMANIA See also: ANAFRANIL (ANGSTSTOORNISSEN, onder Medication) See also: SYNDROOM van TOURETTE TOURETTE"s SYNDROME TS See also: OBSESSIEF-COMPULSIEVE PERSOONLIJKHEIDSSTOORNIS OBSESSIVE-COMPULSIVE PERSONALITY DISORDER Angst- en Paniekstoornissen Angststoornissen - Obsessief-compulsieve stoornis OCD Vriendenkring ... Obsessive-Compulsive Disorders (OCD) page DWARSLAESIE Functionele Neurochirurgie: Dwarslaesie Stichting De Schakel - vereniging van en voor mensen met een dwarslaesie Dwarslaesie: Uitleg Dwarslaesie Links DWERGGROEI DWARFISM SHORT PEOPLE KLEINE MENSEN See also: BOTZIEKTES BONE DISEASES See also: DYSPLASIA See also: ACHONDROPLASIE ACHONDROPLASIA See also: CARTILAGE-HAIR HYPOPLASIA See also:

59. Misa-e My parents were told I have a very rare type of disease called RussellSilver( or sometimes called silver-russell) syndrome. They http://www1.accsnet.ne.jp/~nagakawa/misa-e.html

Russell-Silver Syndrome January 12, 2000 Hello, everybody!!! Welcome to Misa's Home Page!!! My name is Misa. And My mom and Junko are friends. Starting from today, I want to talk about myself and the disease. My mom is a nurse and very positive in learning about the syndrome I am suffering from. So, I think I may write a little and my mom is going to write a lot more eventually. I am now 5 years and 10 months old. But I am only 89cm tall. I couldn't grow right when I was in my mommy's tummy. And also after I was born, I couldn't drink or eat any food like other normal babies. I had a lot of difficulty in taking food. My parents were told I have a very rare type of disease called Russell-Silver ( or sometimes called Silver-Russell) Syndrome. They say there only 33 cases reported in Japan so far. My mom and dad seem to feel O.K. now in accepting what I am. But still they are thinking the way how I can grow a little bit better. I think it's quite all right with this height. But I sometimes feel sad when somebody calls me "Shortie!" Today I came to Aunt Junko's house. She let me play with her computer and I really liked it. I particularly liked Kabu-san's Home Page linked through Kayuchan-chi's Home Page. Kabu-san made his page like a music shop. I kept listening to the theme songs of TV animation while Mom and Junko were talking. I've learned how to use the mouse to click. I wish I had a PC of my own!

60. Ask Jeeves: Search Results For "Types Of Genetic Disorders" http//habitant.org/genetics.htm 5. RusselSilver syndrome Russell-Silver syndrome,(RSS) silver-russell yndrome, Silver syndrome, Russell syndrome http//www http://webster.directhit.com/webster/search.aspx?qry=Types Of Genetic Disorders

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