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。 - Suppr

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超能文献

Congenital localized absence of skin and associated abnormalities resembling epidermolysis bullosa. A new syndrome.

作者信息

Bart B J, Gorlin R J, Anderson V E, Lynch F W

出版信息

Arch Dermatol. 1966 Mar;93(3):296-304.

PMID:5910871

Abstract

摘要

相似文献

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。

Arch Dermatol. 1966 Mar;93(3):296-304.

[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.

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.

[Bart syndrome--separate entity or a variant of epidermolysis bullosa?].[巴特综合征——独立疾病还是大疱性表皮松解症的一种变异型？]

Hautarzt. 1997 Sep;48(9):640-4. doi: 10.1007/s001050050637.

[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.

[Aplasia cutis congenita, epidermolysis bullosa and ungual dystrophy].

An Esp Pediatr. 1998 Sep;49(3):294-6.

[Congenital circumscribed skin aplasia - a rare developmental anomaly of the skin].先天性局限性皮肤发育不全——一种罕见的皮肤发育异常

Pediatr Pol. 1980 Nov;55(11):1233-6.

Generalized atrophic benign epidermolysis bullosa.泛发性萎缩性良性大疱性表皮松解症

Arch Dermatol. 1982 Jun;118(6):375-84.

[Dominant dystrophic epidermolysis bullosa with localized congenital absence of the skin. A case with an ultrastructure study].

Ann Dermatol Venereol. 1986;113(8):697-700.

Congenital localized absence of skin, blistering and nail abnormalities, a new syndrome.先天性局限性皮肤缺失、水疱形成及指甲异常，一种新综合征。

Birth Defects Orig Artic Ser. 1971 Jun;7(8):118-20.

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Aplasia Cutis Congenita of the Lower Limb: A Case Report.下肢先天性皮肤发育不全：一例报告

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Twin Neonates With Bart's Syndrome.患有巴氏综合征的双胎新生儿。

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Bart's syndrome associated with a disorder of sexual differentiation: An atypical presentation in a Cameroonian newborn.伴有性分化障碍的巴特综合征：喀麦隆一名新生儿的非典型表现。

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