一例巴特综合征病例报告。
A case report of Bart syndrome.
作者信息
Sharif Seyed Amirabbas, Mohammadzadeh Alieh, Heidari Mohammad Mahdi, Por Rasoul Etesam
机构信息
Department of Pediatric Kashan University of Medical Sciences Kashan Iran.
Student Research Committee Kashan University of Medical Sciences Kashan Iran.
出版信息
Clin Case Rep. 2023 Jun 26;11(6):e7612. doi: 10.1002/ccr3.7612. eCollection 2023 Jun.
Abstract
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.
摘要
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。
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引用本文的文献
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本文引用的文献
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Twin Neonates With Bart's Syndrome.患有巴氏综合征的双胎新生儿。
Cureus. 2022 Jan 18;14(1):e21363. doi: 10.7759/cureus.21363. eCollection 2022 Jan.
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Recognizable neonatal clinical features of aplasia cutis congenita.先天性表皮发育不全的可识别新生儿临床特征。
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A Case of Aplasia Cutis Congenita Type VI: Bart Syndrome.一例VI型先天性皮肤发育不全：巴特综合征。
Case Rep Dermatol. 2017 Aug 3;9(2):112-118. doi: 10.1159/000478889. eCollection 2017 May-Aug.
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Type VI Aplasia Cutis Congenita: Bart's Syndrome.VI型先天性皮肤发育不全：巴特综合征。
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Bart syndrome with ear malformation.伴有耳部畸形的巴特综合征。
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Congenital localized absence of skin and associated abnormalities resembling epidermolysis bullosa. A new syndrome.先天性局限性皮肤缺失及类似大疱性表皮松解症的相关异常。一种新综合征。
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A mechanobullous disease of the newborn. Bart's syndrome.
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