أعرض تسجيلة المادة بشكل مبسط
| 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 |
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