[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]
[Epidermolysis bullosa and congenital skin aplasia (Bart's syndrome). Report of 3 cases].
作者信息
Tincopa-Wong O W, Peláez-Gutiérrez R, Esparza-Urtecho W, Meléndez-Guevara G, Paoli-Razuri C, Sánchez-Aznarán N
机构信息
Servicio de Dermatología, Hospital Regional, Victor Lazarte Echegaray, Trujillo, Perú.
出版信息
Med Cutan Ibero Lat Am. 1988;16(2):149-54.
The association of epidermolysis bullosa (EB), congenital localized absence of skin and nail alterations like anonychia and dystrophy has been denominated Bart's syndrome, which was described nineteen years ago, and associated with simple, junctional and dystrophies epidermolysis bullosa. We explain in this study three cases, which because of their clinic characteristics will correspond to this new entity. All of these cases happened in the city of Trujillo, Peru.
大疱性表皮松解症（EB）、先天性局限性皮肤缺失以及诸如无甲症和甲营养不良等指甲改变之间的关联被命名为巴特综合征，该综合征于19年前被描述，并与单纯性、交界性和营养不良性大疱性表皮松解症相关。在本研究中，我们阐述了三例因其临床特征而符合这一新病症的病例。所有这些病例均发生在秘鲁的特鲁希略市。
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