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Silver-Russell Syndrome: A Case Report

A 15-year-old male boy with hemihypertrophy (left side) of the body was admitted in the hospital with the history of repeated attacks of convulsion. The patient was diagnosed as Silver-Russell syndrome on clinical ground. Silver-Russell syndrome (SRS) is a very rare genetic disorder that appears no...

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Detalles Bibliográficos
Autores principales: Kumar, Sunil, Jain, AP, Agrawal, Sachin, Chandran, Sindu
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2585578/
https://www.ncbi.nlm.nih.gov/pubmed/18992170
http://dx.doi.org/10.1186/1757-1626-1-304
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author Kumar, Sunil
Jain, AP
Agrawal, Sachin
Chandran, Sindu
author_facet Kumar, Sunil
Jain, AP
Agrawal, Sachin
Chandran, Sindu
author_sort Kumar, Sunil
collection PubMed
description A 15-year-old male boy with hemihypertrophy (left side) of the body was admitted in the hospital with the history of repeated attacks of convulsion. The patient was diagnosed as Silver-Russell syndrome on clinical ground. Silver-Russell syndrome (SRS) is a very rare genetic disorder that appears no later than early childhood. This is usually characterized by asymmetry in the size of the two halves or other parts of the body. Silver-Russell Syndrome occurs mostly in isolated cases because of sporadic genetic changes (mutations) for no apparent reason. For lack of facilities we were not able to do genetic study.
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spelling pubmed-25855782008-11-21 Silver-Russell Syndrome: A Case Report Kumar, Sunil Jain, AP Agrawal, Sachin Chandran, Sindu Cases J Case Report A 15-year-old male boy with hemihypertrophy (left side) of the body was admitted in the hospital with the history of repeated attacks of convulsion. The patient was diagnosed as Silver-Russell syndrome on clinical ground. Silver-Russell syndrome (SRS) is a very rare genetic disorder that appears no later than early childhood. This is usually characterized by asymmetry in the size of the two halves or other parts of the body. Silver-Russell Syndrome occurs mostly in isolated cases because of sporadic genetic changes (mutations) for no apparent reason. For lack of facilities we were not able to do genetic study. BioMed Central 2008-11-09 /pmc/articles/PMC2585578/ /pubmed/18992170 http://dx.doi.org/10.1186/1757-1626-1-304 Text en Copyright © 2008 Kumar et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kumar, Sunil
Jain, AP
Agrawal, Sachin
Chandran, Sindu
Silver-Russell Syndrome: A Case Report
title Silver-Russell Syndrome: A Case Report
title_full Silver-Russell Syndrome: A Case Report
title_fullStr Silver-Russell Syndrome: A Case Report
title_full_unstemmed Silver-Russell Syndrome: A Case Report
title_short Silver-Russell Syndrome: A Case Report
title_sort silver-russell syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2585578/
https://www.ncbi.nlm.nih.gov/pubmed/18992170
http://dx.doi.org/10.1186/1757-1626-1-304
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