Kurtulgan, Hande Küçük Cumhuriyet Üniversitesi - Tıp Fakültesi - Tıbbi Genetik Anabilim Dalı, Turkey , Bolat, Fatih Cumhuriyet Üniversitesi - Tıp Fakültesi - Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Turkey , Göktolga, Gülseren Erkoca Cumhuriyet Üniversitesi - Tıp Fakültesi - Tıbbi Genetik Anabilim Dalı, Turkey , Akkuş, Nejmiye Cumhuriyet Üniversitesi - Tıp Fakültesi - Tıbbi Genetik Anabilim Dalı, Turkey , Çitli, Şenol Cumhuriyet Üniversitesi - Tıp Fakültesi - Tıbbi Genetik Anabilim Dalı, Turkey , Sezgin, İlhan Cumhuriyet Üniversitesi - Tıp Fakültesi - Tıbbi Genetik Anabilim Dalı, Turkey

A neonate with Adams Oliver syndrome: A case report and review of the literature

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Adams Oliver syndrome was first described by Adams and Oliver in 1945. It is a syndrome characterized by aplasia cutis congenita and terminal transverse limb defects of variable severity. A one-day-old female neonate was admitted to the neonatal intensive care unit with aplasia cutis congenita and limb defects. The diagnosis of Adams Oliver syndrome was based on the typical disease features, together with typical appearances on radiography. In this case report, we present a case diagnosed with Adams Oliver syndrome and we also discuss the clinical findings of patients with Adams Oliver syndrome reported in the literature.

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Adams Oliver syndrome , aplasia cutis congenita , clinical features , limb defects

Cumhuriyet Medical Journal

579