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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Dicle University Medical School
2004-01-01
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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 |
work_keys_str_mv |
AT alpaslantuzcu afamilywithrusselsilversyndromeacasereport AT hasankayabası afamilywithrusselsilversyndromeacasereport AT mithatbahceci afamilywithrusselsilversyndromeacasereport AT bulentyılmaz afamilywithrusselsilversyndromeacasereport AT ergunparmaksız afamilywithrusselsilversyndromeacasereport AT alpaslantuzcu familywithrusselsilversyndromeacasereport AT hasankayabası familywithrusselsilversyndromeacasereport AT mithatbahceci familywithrusselsilversyndromeacasereport AT bulentyılmaz familywithrusselsilversyndromeacasereport AT ergunparmaksız familywithrusselsilversyndromeacasereport |
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