Sharif Seyed Amirabbas, Mohammadzadeh Alieh, Heidari Mohammad Mahdi, Por Rasoul Etesam
Department of Pediatric Kashan University of Medical Sciences Kashan Iran.
Student Research Committee Kashan University of Medical Sciences Kashan Iran.
Clin Case Rep. 2023 Jun 26;11(6):e7612. doi: 10.1002/ccr3.7612. eCollection 2023 Jun.
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.
巴特综合征是一种罕见病症，其特征为大疱性表皮松解症（EB）、皮肤发育不全（AC）和指甲异常。先天性皮肤发育不全VI型于1966年由巴特等人首次描述。本文报告了一名阿富汗男婴患有耳部畸形的巴特综合征病例。据作者所知，这是阿富汗家族中报告的首例巴特综合征病例。
