Çaksen, HKurtoglu, S2025-05-102025-05-1020020385-24071346-813810.1111/j.1346-8138.2002.tb00285.x2-s2.0-0036307028https://doi.org/10.1111/j.1346-8138.2002.tb00285.xhttps://hdl.handle.net/20.500.14720/14554Kurtoglu, Selim/0000-0002-5256-0128Aplasia cutis congenita is a rare disorder characterized by developmental absence of skin on the scalp as multiple or solitary, noninflammatory. Well demarcated, oval or circular 1- to 2-cm ulcers. The disease may be isolated or associated with anomalies of the skin, eyes, ear-nose-neck and limbs, developmental defects of the cardiovascular, gastrointestinal, genitourinary and central nervous systems, and malformation syndromes such as chromosomal abnormalities. Adams-Oliver syndrome, Bart's syndrome, and Johanson-Bilzzard syndrome. In this article, five newborn infants with aplasia ctius congenita (one associated with Adams-Oliver syndrome and another concomitant with Bart's syndrome) are reported because of their rare presentation in the literature.eninfo:eu-repo/semantics/closedAccessAplasia Cutis CongenitaBart'S SyndromeNewbornArticle296Q2Q137637912126077WOS:000176498000012