Karaman, AliKahveci, HasanLaloğlu, Fuat2020-05-072020-05-072011-02-23Karaman, A. vd. (2011). "Greig cephalopolysyndactyly syndrome: A case report". Güncel Pediatri, 9(1), 47-49.1304-90541308-6308https://dergipark.org.tr/tr/download/article-file/904908http://hdl.handle.net/11452/10569Introduction: 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.Giriş: Greig sefalopolisindaktili sendromu (GCPS), çoklu konjenital anomalili bir pleiotropik sendromdur. Olgu Sunumu: Hasta yüksek alın, frontal şişlik, makrosefali, belirgin hipertelorizm, aşağı eğik palpebral fissürler ve geniş bir burun köküne sahipti. Ayakları bilateral kutanöz sindaktilili polidaktili gösterdi. Tartışma: GCPS otozomal dominant genetik modelli nadir bir durumdur. Primer bulguları, hipertelorizm, frontal şişliği olan makrosefali ve polisindaktiliyi içerir. Burada, GCPS’nin tipik klinik bulguları ile 1 haftalık kız bir olgu sunuldu.trinfo:eu-repo/semantics/openAccessGreig cephalopolysyndactyly syndromeMacrocephalyPolysyndactylyGreig sefalopolisindaktili sendromuMakrosefaliPolisindaktiliArticle474991