Extractions: A syndrome of intra-uterine dwarfism with low birth weight characterized by short stature, skeletal asymmetry, relatively large skull with triangular shaped head, small incurved little fingers, characteristic facies, precocious sexual development. Renal and/or ureteral defects and mental retardation may occur in some cases. Café au lait macules are present in nearly half the cases. Nephroblastoma can be a complication. No sex preponderance. The mode of inheritance is unknown.
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Extractions: AUTHOR INFORMATION Section 1 of 11 Authored by Ainu Prakash-Cheng, MD, PhD , Assistant Professor of Human Genetics and Pediatrics, Department of Human Genetics, Mount Sinai School of Medicine Coauthored by Margaret McGovern, MD, PhD , Vice Chair, Associate Professor, Department of Human Genetics, Mount Sinai School of Medicine Ainu Prakash-Cheng, MD, PhD, is a member of the following medical societies: American Academy of Pediatrics American Society of Gene Therapy , and American Society of Human Genetics Edited by Elaine H Zackai, MD , Director of Clinical Genetics Center, Professor of Pediatrics, Department of Pediatrics, Division of Human Genetics and Molecular Biology, University of Pennsylvania, Children's Hospital of Philadelphia; Robert Konop, PharmD , Clinical Assistant Professor, Department of Pharmacy, Section of Clinical Pharmacology, University of Minnesota;
Health Library Find Information On Russell-Silver Syndrome At Find information on russellsilver syndrome at MerckSource. Learnmore about russell-silver syndrome. Definition A condition of http://www.mercksource.com/pp/us/cns/cns_hl_adam.jspzQzpgzEzzSzppdocszSzuszSzcns
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The Health Library Genetics And Birth Defects russellsilver syndrome. russell-silver syndromeMAGIC Foundation. russell-silversyndromeNORD. russell-silver syndromeGeneReviews, University of Washington. http://healthlibrary.stanford.edu/resources/internet/bodysystems/genetics5.html
Extractions: Diseases and Disorders Use these links to jump directly to your topic of interest: Birth Defects (General) Cardiovascular Defects Chromosome Disorders Connective Tissue Disorders ... Nervous System Defects Genetics and Birth Defects: Page 1 Page 2 Page 3 Page 4 Dwarfism Dwarfism:MEDLINEplus Dwarfism Types and Definitions:Little People of America Frequently Asked Questions (about Dwarfism):Little People of America The MAGIC Foundation for Children's Growth and Related Adult Disorders ... Skeletal Dysplasia Clinical Summaries:Greenberg Center for Skeletal Dysplasias, Johns Hopkin Achondroplasia Achondroplasia:March of Dimes Achondroplasia:Greenberg Center for Skeletal Dysplasias Achondroplasia:GeneReviews, University of Washington Cockayne Syndrome Frequently Asked Questions About Cockayne Syndrome:Cockayne Syndrome Network Genes and Disease: Cockayne Syndrome:NCBI Cockayne Syndrome:GeneReviews, University of Washington Diastrophic Dysplasia Diastrophic Dysplasia:Greenberg Center for Skeletal Dysplasias Genes and Disease: Diastrophic Dysplasia:NCBI Ellis-van Creveld Syndrome Ellis-van Creveld Syndrome:Greenberg Center for Skeletal Dysplasias Genes and Disease: Ellis-van Creveld Syndrome:NCBI Russell-Silver Syndrome Russell-Silver Syndrome:MAGIC Foundation Russell-Silver Syndrome:NORD Russell-Silver Syndrome:GeneReviews, University of Washington
Raisingkids: Ask Our Experts - Silver-Russell Syndrome Ask Our Experts silverrussell syndrome David's advice russell-silversyndrome (RSS) has a number of recognised characteristics. http://www.raisingkids.co.uk/ask/ex03_pri01.asp
Extractions: My son has been fed though a gastrostomy since he was 3 months old and now he won't eat. He gets 1000 ml of 'Nutrini Extrain' his feeding pump at night but he's still underweight and doesn't put on weight well. He also has Silver-Russell Syndrome and a curved spine - could this have anything to do with it? If not, have you any suggestions on how to help? He is 5 yrs-old now, and I don't get any answers from anybody. David's advice Russell-Silver syndrome (RSS) has a number of recognised characteristics. Some individuals have many of the documented traits, while others have very few. Almost every individual with the syndrome has: Beyond this the characteristics vary very widely. However, the early years are often the most difficult and typically appetite will improve with age.
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Extractions: Children with Russell-Silver syndrome generally achieve less than 5 feet at adult height. Side-to-side asymmetry is fairly common. 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 curved the fingers, and pigmented skin lesions called cafe-au-lait spots
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Online And Offline Support: R Homepage address http//www.tucson.com/rts/. russellsilver syndrome. Associationfor Children with russell-silver syndrome, Inc. http://www.widesmiles.org/support/r.html
Extractions: R Robinow Syndrome Robinow Syndrome Foundation Romberg Syndrome/Parry-Romberg Syndrome The Rombergs Connection and The Romberg's Connection Annex Rubinstein-Taybi Syndrome Please note: Children, teens, and adults with Rubinstein-Taybi Syndrome have specific facial features that do not require reconstructive surgery. Rubinstein-Taybi Parent Group (RTPG) People served: Parents of children with Rubinstein-Taybi Syndrome Services provided: Support, parent-matching, information, and newsletter Address: PO Box 146, Smith Center KS 66967 Phone number: (785) 697-2984 Contact people: Garry and Lorrie Baxter Email address: lbaxter@ruraltel.net
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Silver-Russell Syndrome, Ascertainment Of Uniparental Disomy silverrussell syndrome, ascertainment of uniparental disomy. Molecular geneticand clinical investigations of more than 100 patients and their families. http://www.research-projects.unizh.ch/med/unit42200/area313/p2319.htm
Extractions: research project Silver-Russell syndrome, ascertainment of uniparental disomy Molecular genetic and clinical investigations of more than 100 patients and their families. Contacts Prof. A. Schinzel (Project Leader) schinzel@medgen.unizh.ch Dr. A. Baumer (Project Leader) baumer@medgen.unizh.ch Dr. M. Riegel Supported By Companies Last Update Responsible Project Leader: Prof. A. Schinzel, Dr. A. Baumer Professor or Research Area Leader: Prof. Dr. Albert Schinzel Institute or Clinic: Faculty: Use the Eurospider retrieval system to find similar projects Use the Eurospider retrieval system to search the research report For authorized person(s) only Comments to uni research page generation 06.03.2003
1653 Russell-Silver Syndrome Identification Of A Candidate russellsilver syndrome Identification of a candidate region on the short arm ofchromosome 7. BA Fernandez 1 , I. Teshima 1 , K. Nakabayashi 1 , V. Proud 2 http://www.faseb.org/genetics/ashg99/f1653.htm