81. Silver Russell Syndrome Silver Russell syndrome. A Medical General Hospital. A resource with informationon over 4000 medical topics including Silver Russell syndrome. http://www.marylandemphysema.com/medical-terms/03137.htm

Silver Russell syndrome A Medical Encyclopedia Article provided by Maryland General Hospital A resource with information on over 4000 medical topics including: Silver Russell syndrome Previous Next

82. UK Self Help Groups: R RTS Support Group, Tel 01568 720 350. RussellSilver syndrome. contactSilver-Russell Group c/o Child Growth Foundation, Tel 020 8995 0257. http://www.ukselfhelp.info/r.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). Rare Chromosome Disorders UNIQUE (Rare Chromosome Disorders Support Group) , Tel 01883 330 766 Raynaud's , Tel 01270 872 776 Reflex Anoxic Seizure/Reflex Asystolic Syncope STARS (Syncope Trust And Reflex Anoxic Seizure) , Tel 01789 450 564 Reflex Sympathetic Dystrophy/Complex Regional Pain Syndrome RSD/CRPS Group , Tel 01484 643 458 Reifenstein Syndrome contact Androgen Insensitivity Support Group , Helpline 01295 670 140 Relapsing Polychondritis Relapsing Polychondritis UK Rendu-Osler-Weber Syndrome contact Telangiectasia Group , Tel 01494 528 047 Repetitive Strain Injury RSI Association , Tel 020 7266 2000/Helpline 0800 018 5012 RSI Self Help Group , Tel 020 8800 5049 Restless Leg Syndrome contact Ekbom's Support Group Restricted Growth contact Child Growth Foundation , Tel 020 8995 0257 also Restricted Growth Association Retinitis Pigmentosa British Retinitis Pigmentosa Society , Tel 01280 821 334 Retinoblastoma contact Retinoblastoma Society , Tel 020 7600 3309 Rett Syndrome National Rett Syndrome Association, Tel 0141 641 7662

83. Alice Translate this page a pour objet d’apporter un réconfort moral et un soutien matériel et financieraux familles ayants des enfants souffrant du syndrome SILVER RUSSELL (RSS/SRS http://users.skynet.be/vitoux.auderghem/images/Liens/alice/alice.htm

Je m’appelle Alice et je suis atteinte du syndrome de Silver-Russell. Les principales caractéristiques de ce syndrome chez moi sont : déficit au niveau du système nerveux central, anorexie, reflux gastro-oesophagien (avec troubles de la motilité gastrique), retard de croissance, hypoglycémie, déficience en hormone de croissance, difficultés respiratoires, petite taille. En conséquence, j’ai besoin de différents traitements comme l’alimentation par sonde gastrique de gavage 24h./24 h. J'ai un tube qui sort de mon petit ventre et qui est raccordé à une pompe que je porte en permanence dans un sac à dos. J’ai aussi subi plusieurs opérations, dois suivre un traitement: aux hormones de croissance, antibiotique, zantac, prépulsite, pulmicort, fer, lactulose, faire de la kiné respiratoire et de la psychomotricité. Plus tard, d’autres traitements seront nécessaires (logopédie, orthopédie et autres). Pour mon bien être et mon bon développement, nous devons nous rendre 1 à 2 fois par an aux USA pour rencontrer le Dr. Madeleine

84. Institute Of Reproductive And Developmental Biology | Research Groups | Molecula Silver Russell syndrome Silver Russell syndrome (SRS) is characterised byintrauterine and postnatal growth restriction with lateral asymmetry. http://www.med.ic.ac.uk/divisions/58/molecular_genetics_growth.asp

Introduction Research Groups Staff List Postgraduate Opportunities ... Imperial College Molecular Genetics of Growth and Development Group Heads Dr. Gudrun Moore (Reader in Molecular Biology) Dr. Philip Stanier (Senior Lecturer) Professor Michael Preece (Institute of Child Health) (Honorary Chair at IC) Dr. Pamela Johnson (Honorary Senior Lecturer and Consultant in Fetal Medicine) PostDocs: Dr. Kit Doudney Dr. Claire Braybrook Dr. Megan Hitchins Research Assistants Louise Bentley David Monk Sophia Apostolidou Principal Aims To identify genes that are involved in key processes in fetal development that when disrupted cause common human disorders Cleft palate Cleft palate research is carried out in collaboration with Dr. Alfred Arnason and Professor Arni Bjornsson in Reykjavik, Iceland. Genomic contiging and sequencing is performed in association with Dr. Mark Ross at the Sanger Centre, Cambridge. Key Publications Stanier, P., Forbes, S.A., Arnason, A., Bjornsson, A., Sveinbjornsdottir, E., Williamson, R. and Moore, G.E. (1993). The localisation of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X. Genomics Forbes, S.A., Brennan, L., Richardson, M., Coffey, A., Bentley, D., Mumm, S., Moore, G.E. and Stanier, P. (1996). Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.

85. Listings Of The World Health Conditions And Diseases Genetic The CaF Directory Post Review A definition of Silver Russell syndrome,its inheritance patterns, and prenatal diagnosing. Also http://listingsworld.com/Health/Conditions_and_Diseases/Genetic_Disorders/Russel

86. Diet, Health, Diseases, Vitamins Iwant2bhealthy.com Factsheets, meetings and newsletter. · RUSSELLSILVER syndrome contact Silver-Russellsyndrome Support Group c/o Child Growth Foundation under Growth. http://www.iwant2bhealthy.com/supportgroups/index_r.shtml

location: support groups healthy iwant2b.com Support groups Reflex anoxic seziure Repetitive strain injury Rheumatism Road death and injury Support groups quick finder Aids / HIV Anorexia Arthritis Asthma ... P Q R S T U ... X Y Z Information supplied by g-text FREEPOST NWW6775, BLACKPOOL. FY4 3GA. RADIOTHERAPY EXPOSURE/INJURY RIPS (Radiotherapy Injured Patients Support ) – Cindy Ricketts, 194 Colchester Road, Lawford, Essex, CO11 2BP.  Tel 01206 395 610.  Information and support to those who have been damaged by radiotherapy. RARE CHROMOSOME DISORDERS UNIQUE (Rare Chromosome Disorder Support Group) – Beverly Searle, PO Box 2189, Caterham, CR3 5GN.  Tel/Fax 01883 330 766.  Support and information for families and interested professionals.  www.rarechromo.org rarechromo@aol.com RAYNAUD'S – 112 Crewe Road, Alsager, Cheshire, ST7 2JA.  Tel 01270 872 776.  Provides information and advice, support and literature. www.raynaud’s.demon.co.uk webmaster@raynaud’s.demon.co.uk REFLEX ANOXIC SEIZURE STARS (SYNCOPE TRUST AND REFLEX ANOX-IC SEIZURES) PO Box 175, Stratford-Upon-Avon, CV37 8YD.  Tel/Fax 01789 450 564.

87. Russell-Silver Syndrome - Overview RussellSilver syndrome. Alternative names Silver Russell syndrome;Silver syndrome. Definition A condition of unknown origin, but http://www.audrainmedicalcenter.com/ency/article/001209.htm

Disease Injury Nutrition Poison ... Prevention Russell-Silver syndrome Definition: A condition of unknown origin, but which is characterized by short stature and frequent asymmetry in the size of 2 halves or parts of the body. Alternative Names: Silver Russell syndrome; Silver syndrome Causes, incidence, and risk factors: Genetic problems are thought to cause this syndrome although the specific gene(s) remain to be discovered. The pattern of inheritance has not been determined but in most cases it seems sporadic, that is to say, there is no family history in preceding generations/siblings. Children with Russell-Silver syndrome are born small and generally achieve less than 5 feet at adult height. Side-to-side asymmetry is fairly common, for example a left body part may be larger than the right counterpart. This asymmetry may occur anywhere including the face. Other findings include excessive sweating , a small triangular face which makes the skull look large by comparison, inward curving 5th fingers, and pigmented skin lesions called cafe-au-lait spots Review Date: 9/10/2001 Reviewed By: David G. Brooks, M.D., Ph.D., Division of Medical Genetics, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

88. Medicalseek - Search Engine For The Healthcare Industry stepstn.com/cgiwin/nord.exe?proc=GetDo The CaF Directory A definition of SilverRussell syndrome, its inheritance patterns, and pre-natal diagnosing. http://www.medicalseek.net/Conditions_and_Diseases_Genetic_Disorders_Russell_Sil

CATEGORIES ADD A LINK ADVERTISE CONTACT US ... Genetic Disorders Russell Silver Syndrome Conditions and Diseases:Genetic Disorders:Russell Silver Syndrome NORD - Russell Silver Syndrome Offers a general discussion, the synonyms and further resources. stepstn.com/cgi-win/nord.exe?proc=GetDo... The CaF Directory A definition of Silver Russell syndrome, its inheritance patterns, and pre-natal diagnosing. Also lists a support group in the United Kingdom. cafamily.org.uk/Direct/s30.html CATEGORIES ADD A LINK ADVERTISE CONTACT US ... FORUMS

89. Prof. Dr. Albert Schinzel Origin of balanced translocations which arose de novo. SilverRussellsyndrome, ascertainment of uniparental disomy. Sonderegger. Chromosome http://www.research-projects.unizh.ch/med/unit42200/area313/

research area Prof. Dr. Albert Schinzel Current Research Projects by Project Leaders N.N. Candidate genes for psychiatric disorders (schizophrenia and bipolar psychosis) Hanauer Mutation analysis in Coffin-Lowry syndrome patients Mutation analysis in Coffin-Lowry syndrome patients Hergersberg Mutation analysis in X-linked diseases: Rett syndrome, McLeod syndrome, and fragile X-Syndrome Mutation analysis in X-linked diseases: Deletion analysis on the X chromosome Mutation analysis in the neurofibromatosis 2 gene Mutation analysis in the HLXB9 gene in the DNA of probands with anal sphincter dysplasia ... Localization of genes for inherited ophthalmological syndromes Schinzel Investigation of the origin of de novo extra chromosomes and structural rearrangements through chromosome dissection and reverse painting Clinical delineation of malformation syndromes of genetic etiology Human Cytogenetic Database and Catalogue of Chromosome Aberrations in Man The contribution of Connexin26 mutations to severe congenital sensori-neural deafness Schinzel / Baumer Prader-Willi syndrome and Angelman syndrome: ascertainment of deletions, uniparental disomy, imprinting defects, UBE3A mutations

90. Biblio2_pediatría Y Puericultura http://www.pypweb.com/biblio2.htm

Bibliografía: Síndrome de Silver Russell. 1 Rivas Crespo M F, Alvarez F J, De la Rúa VR, Crespo Hernández MC.Síndrome de Silver-Russell. Rev Esp Pediatr,1987; 43: 23-32. 2 Rodriguez Hierro F. Casos clínicos. Pediatría I . Ediciones científicas y técnicas S. A. Barcelona, 1992: 35-39 3 Delgado A, Santolaya J M, Arístegui J. Hipocrecimientos dismórficos. En Monografías de Pediatría, Crecimiento y Desarrollo Tomo II. Jarpyo Editores. Madrid-Barcelona, 1985: 22-24. 4 Wiedemann H R. Síndrome de Silver. Sindrome de Russell. En El Síndrome Característico. Ed Ancora, Barcelona 1985:109. 5 Argemí Renom J. Diagnóstico de los retrasos de crecimiento. En Monografías de la Catedra de Pediatría de Barcelona. Prof. M. Cruz Hernandez. Ed Espax, Barcelona 1978:157. 6 Argente Oliver J. Fundamentos genético-hormonales en la regulación del crecimiento humano. An Esp Pediatr, 1996; Supl 79: 39-43. 7 Bueno M. et al.Crecimiento y desarrollo humanos y sus trastornos. 2ª Ed. Ediciones Ergon SA, 1996:125,142,189-191. 8 Wollmann HA, Kirchner T, Enders H, Preece MA, Ranke MD. Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients. Eur J Pediatr 1995; 154:958-968.

91. SpringerLink: Human Genetics - Abstract Volume 100 Issue 3/4 (1997) Pp 415-419 Abstract Volume 100 Issue 3/4 (1997) pp 415419. Molecular studies in 37 Silver-Russellsyndrome patients frequency and etiology of uniparental disomy. http://dx.doi.org/10.1007/s004390050526

Human Genetics ISSN: 0340-6717 (printed version) ISSN: 1432-1203 (electronic version) Table of Contents Abstract Volume 100 Issue 3/4 (1997) pp 415-419 Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy T. Eggermann (1), Hartmut A. Wollmann (2), Ruprecht Kuner (1), Katja Eggermann (1), Herbert Enders (1), Peter Kaiser (1), Michael B. Ranke (2) Received: 13 February 1997 / Accepted: 13 May 1997 Abstract Article in PDF-Format Online publication: August 5, 1997 helpdesk.link@springer.de

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