A Family with Russel Silver Syndrome: A Case Report

Russel Silver Syndrome (RSS) is a very rare syndrome with phenotypicchanges and its etiology has not explained yet. In 1953 and 1954, a specialgroup of Intrauterin Growth Reterdation, childiren with short staturealong a small triangular face, low-set ears, incurved fifth fingers and othercharactheri...

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Main Authors: Alpaslan Tuzcu, Hasan Kayabaşı, Mithat Bahçeci, Bülent Yılmaz, Ergün Parmaksız
Format: Article
Language:English
Published: Dicle University Medical School 2004-01-01
Series:Dicle Medical Journal
Subjects:
Online Access:http://4181.indexcopernicus.com/fulltxt.php?ICID=887961
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spelling doaj-1f9842784b8140998473bc3325af3ea92020-11-24T22:52:27ZengDicle University Medical SchoolDicle Medical Journal 1300-29451308-98892004-01-013143437A Family with Russel Silver Syndrome: A Case ReportAlpaslan TuzcuHasan KayabaşıMithat BahçeciBülent YılmazErgün ParmaksızRussel Silver Syndrome (RSS) is a very rare syndrome with phenotypicchanges and its etiology has not explained yet. In 1953 and 1954, a specialgroup of Intrauterin Growth Reterdation, childiren with short staturealong a small triangular face, low-set ears, incurved fifth fingers and othercharactheristics were described. Our patient who come us with shortstature was a twenty years old man. His parents were relatives and he wasthe second child of a family with six children. His length was 155 cm, under-3SD. Also he had a small triangular face, his lips were towards downrightand a small mandibula. Incurved fifth fingers and short stature werepresent in all members of the family.As the result, RSS must be thought inpatients with short sature, especially who has similar phenotypicspecialities as our patient.http://4181.indexcopernicus.com/fulltxt.php?ICID=887961Russel Silver Syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Alpaslan Tuzcu
Hasan Kayabaşı
Mithat Bahçeci
Bülent Yılmaz
Ergün Parmaksız
spellingShingle Alpaslan Tuzcu
Hasan Kayabaşı
Mithat Bahçeci
Bülent Yılmaz
Ergün Parmaksız
A Family with Russel Silver Syndrome: A Case Report
Dicle Medical Journal
Russel Silver Syndrome
author_facet Alpaslan Tuzcu
Hasan Kayabaşı
Mithat Bahçeci
Bülent Yılmaz
Ergün Parmaksız
author_sort Alpaslan Tuzcu
title A Family with Russel Silver Syndrome: A Case Report
title_short A Family with Russel Silver Syndrome: A Case Report
title_full A Family with Russel Silver Syndrome: A Case Report
title_fullStr A Family with Russel Silver Syndrome: A Case Report
title_full_unstemmed A Family with Russel Silver Syndrome: A Case Report
title_sort family with russel silver syndrome: a case report
publisher Dicle University Medical School
series Dicle Medical Journal
issn 1300-2945
1308-9889
publishDate 2004-01-01
description Russel Silver Syndrome (RSS) is a very rare syndrome with phenotypicchanges and its etiology has not explained yet. In 1953 and 1954, a specialgroup of Intrauterin Growth Reterdation, childiren with short staturealong a small triangular face, low-set ears, incurved fifth fingers and othercharactheristics were described. Our patient who come us with shortstature was a twenty years old man. His parents were relatives and he wasthe second child of a family with six children. His length was 155 cm, under-3SD. Also he had a small triangular face, his lips were towards downrightand a small mandibula. Incurved fifth fingers and short stature werepresent in all members of the family.As the result, RSS must be thought inpatients with short sature, especially who has similar phenotypicspecialities as our patient.
topic Russel Silver Syndrome
url http://4181.indexcopernicus.com/fulltxt.php?ICID=887961
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