Aplasia Kutis Congenita With Multiple Scalp and Limb Locations

Abstract

Aplasia cutis congenita is a rarely seen heterogenous group of disease characterized by the absence of a portion of skin, subdermal tissue, infrequently bone and meninges. Aplasia cutis congenita is typically sporadic; however, syndromic cases have also been reported. In this report, we present sporadic case, two-day old baby who had multiple scalp and extremity defects. We aimed to remind the rare entity in differential diagnosis of scalp defects. © 2021, Pamukkale University. All rights reserved.