1.
Clin Case Rep
; 11(6): e7612, 2023 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37384233
RESUMO
Bart syndrome is a rare condition characterized by epidermolysis bullosa (EB), aplasia cutis (AC), and nail abnormalities. Aplasia cutis congenita type VI was first described in 1966 by Bart et al. This article reports a case of Bart syndrome with ear malformation in a male Afghan newborn. To the authors' knowledge, this is the first case of Bart syndrome reported in an Afghan family.