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http://dspace.mediu.edu.my:8181/xmlui/handle/123456789/6016| Title: | Greig Cephalopolysyndactyly Syndrome: A Case Report Case Report |
| Keywords: | Greig cephalopolysyndactyly syndrome macrocephaly polysyndactyly |
| Issue Date: | 30-May-2013 |
| Publisher: | Galenos Yayincilik |
| 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) |
| URI: | http://koha.mediu.edu.my:8181/jspui/handle/123456789/6016 |
| Other Identifiers: | http://www.doaj.org/doaj?func=openurl&genre=article&issn=13049054&date=2011&volume=9&issue=1&spage=47 |
| Appears in Collections: | Health Sciences |
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