A case report of Bart syndrome

Author:

Sharif Seyed Amirabbas1,Mohammadzadeh Alieh1,Heidari Mohammad Mahdi1ORCID,Por Rasoul Etesam2

Affiliation:

1. Department of Pediatric Kashan University of Medical Sciences Kashan Iran

2. Student Research Committee Kashan University of Medical Sciences Kashan Iran

Abstract

Key Clinical MessageBart 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.

Publisher

Wiley

Subject

General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Bart syndrome: A case report of neonatal disorder;Clinical Case Reports;2024-02

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