Robert’s SyndromeTurhan Topoğlu, Suar Çakı, F. Fetül Ceniz, Fazilet Metin, Sevil ÖzçayGöztepe SSK Hospital, Child Health and Diseases, Istanbul
Robert’s syndrome is a rare autosomal recessive disorder characterized primarily by symmetric reduction anomalies of all lims, prenatal and postnatal growth retardation and craniofacial abnormalities. A diagnosis of Robert’s syndrome clinical and genetical features was made. This disease is presented because it is seen rarely. Keywords: Robert’s syndrome, craniofacial abnormalities, growth retardation
Robert SendromuTurhan Topoğlu, Suar Çakı, F. Fetül Ceniz, Fazilet Metin, Sevil ÖzçayGöztepe SSK Eğitim Hastanesi, Çocuk Sağlığı ve Hastalıkları Kliniği, İstanbul
Anahtar Kelimeler: Robert sendromu, kraniyofasiyal anomaliler, büyüme geriliği
Turhan Topoğlu, Suar Çakı, F. Fetül Ceniz, Fazilet Metin, Sevil Özçay. Robert’s Syndrome. Medeniyet Med J. 2003; 18(1): 52-53
Corresponding Author: Turhan Topoğlu, Türkiye |
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