Greig Cephalopolysyndactyly Syndrome:  A Case Report Case Report

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DC Field	Value	Language
dc.creator	Ali Karaman	-
dc.creator	Hasan Kahveci	-
dc.creator	Fuat Laloğlu	-
dc.date	2011	-
dc.date.accessioned	2013-05-30T14:03:27Z	-
dc.date.available	2013-05-30T14:03:27Z	-
dc.date.issued	2013-05-30	-
dc.identifier		-
dc.identifier	http://www.doaj.org/doaj?func=openurl&genre=article&issn=13049054&date=2011&volume=9&issue=1&spage=47	-
dc.identifier.uri	http://koha.mediu.edu.my:8181/jspui/handle/123456789/6016	-
dc.description	Introduction: The Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome. Case Report: The patient had high forehead, frontal bossing, macrocephaly, apparent hypertelorism, down-slanting palpebral fissures and a broad nasal root. The feet showed bilateral polydactyly with cutaneous syndactyly of the fifth digits. Conclusion: GCPS is a rare condition with an autosomal dominant mode of inheritance. The primary findings include hypertelorism, macrocephaly with frontal bossing, and polysyndactyly. Presented here is a case of a 1 week old female with typical clinical manifestations of GCPS. (Journal of Current Pediatrics 2011; 9: 47-9)	-
dc.publisher	Galenos Yayincilik	-
dc.source	Güncel Pediatri	-
dc.subject	Greig cephalopolysyndactyly syndrome	-
dc.subject	macrocephaly	-
dc.subject	polysyndactyly	-
dc.title	Greig Cephalopolysyndactyly Syndrome: A Case Report Case Report	-
Appears in Collections:	Health Sciences

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