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Congenital localized absence of skin associated with blistering of the skin and mucous membranes: Bart's syndrome.

作者信息

Gharpuray M B, Tolat S N, Patki A H

机构信息

Department of Dermatology, Sassoon General Hospital, Pune, India.

出版信息

Cutis. 1989 Oct;44(4):318-20.

PMID:2805808
Abstract

A newborn girl presented with a congenital localized absence of skin on both legs. At the age of eight months, blistering of the scalp, upper limbs, and oral mucous membranes occurred, which was nonscarring and recurrent. This case is reported because of its rarity.

摘要

相似文献

1
Congenital localized absence of skin associated with blistering of the skin and mucous membranes: Bart's syndrome.
Cutis. 1989 Oct;44(4):318-20.
2
Congenital localized skin defect and epidermolysis bullosa hereditaria letalis.先天性局限性皮肤缺损和致死性遗传性大疱性表皮松解症。
Acta Derm Venereol. 1979;59(6):533-7.
3
[Congenital transient mechanobullous dermatosis (Bart's syndrome). A clinical case and review of the literature].[先天性短暂性机械性大疱性皮肤病(巴特综合征)。1例临床病例及文献复习]
G Ital Dermatol Venereol. 1989 Oct;124(10):447-50.
4
Bart's syndrome associated with pyloric and choanal atresia.伴有幽门闭锁和后鼻孔闭锁的巴特综合征。
Turk J Pediatr. 2013 Mar-Apr;55(2):214-7.
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[Epidermolysis bullosa dystrophica Bart (Bart syndrome)].[营养不良性大疱性表皮松解症巴特型(巴特综合征)]
Hautarzt. 1985 Jun;36(6):351-3.
6
[Epidermolysis bullosa and congenital skin aplasia (Bart's syndrome). Report of 3 cases].[大疱性表皮松解症与先天性皮肤发育不全(巴特综合征)。3例报告]
Med Cutan Ibero Lat Am. 1988;16(2):149-54.
7
Bart's syndrome: a mechanobullous disease of the newborn. Report of five cases and review.巴特综合征:一种新生儿机械性大疱性疾病。5例报告及文献复习
Clin Pediatr (Phila). 1986 May;25(5):252-4. doi: 10.1177/000992288602500503.
8
Congenital absence of skin and blistering in a neonate. Bart's syndrome and mandibulofacial dysostosis.新生儿先天性皮肤缺失和水疱形成。巴特综合征与下颌面部发育不全。
Arch Dermatol. 1995 Oct;131(10):1197, 1200. doi: 10.1001/archderm.131.10.1197.
9
Bart's syndrome: report of a case.
Cutis. 1984 Oct;34(4):410-2.
10
Dystrophic epidermolysis bullosa presenting with congenital localized absence of skin: report of four cases.
Br J Dermatol. 1983 Apr;108(4):477-83. doi: 10.1111/j.1365-2133.1983.tb04603.x.

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