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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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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. |
format | Text |
id | pubmed-2585578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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