2011 Cilt 9 Sayı 1

Permanent URI for this collectionhttps://hdl.handle.net/11452/6401

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Browsing by Author "Laloğlu, Fuat"

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    Greig cephalopolysyndactyly syndrome: A case report
    (Uludağ Üniversitesi, 2011-02-23) Karaman, Ali; Kahveci, Hasan; Laloğlu, Fuat
    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.