Author/Authors :
kale, yusuf gaziantep kadin dogum ve çocuk hastaliklari hastanesi - yeni dogan klinigi, Turkey , bilgiç, ali evren gaziantep kadin dogum ve çocuk hastaliklari hastanesi - yeni dogan klinigi, Turkey , eltan, mehmet gaziantep kadin dogum ve çocuk hastaliklari hastanesi - yeni dogan klinigi, Turkey , köse, ahmet gaziantep kadin dogum ve çocuk hastaliklari hastanesi - pediatrik kardiyoloji klinigi, Turkey , sezer, sadettin gaziantep kadin dogum ve çocuk hastaliklari hastanesi - pediatrik kardiyoloji klinigi, Turkey
Abstract :
Adams Oliver syndrome was first described in 1945. It is a hereditary disease characterised by aplasia cutis congenita, bone defect underlying the scalp and terminal transverse limb defects of variable severity. This case, diagnosed as Adams-Oliver syndrome by physical examination and radiological findings, is presented because of its rarity, with a review of the literature.
NaturalLanguageKeyword :
Adams , Oliver Syndrome , Aplasia Cutis , Extremity Defects , Prematurity
