先天性皮肤发育不全合并并指（趾）畸形及多乳头症：另一例具有相似临床表现家系的报告
Aplasia cutis congenita associated with syndactyly and supernumerary nipples: report of a second family with similar clinical findings.
作者信息
Halper S, Rubenstein D
机构信息
University of Chicago, Department of Medicine, Section of Dermatology, Illinois 60637.
出版信息
Pediatr Dermatol. 1991 Mar;8(1):32-4. doi: 10.1111/j.1525-1470.1991.tb00836.x.
Abstract
Aplasia cutis congenita (ACC) is a rare disorder characterized by localized absence of skin at birth. A subtype consisting of a solitary scalp defect in association with limb abnormalities has been described. We report a case of ACC in association with 3,4 syndactyly and supernumerary nipples with an apparent autosomal dominant inheritance pattern.
摘要
先天性皮肤发育不全（ACC）是一种罕见的疾病，其特征为出生时局部皮肤缺失。一种由孤立的头皮缺损伴肢体异常组成的亚型已被描述。我们报告一例ACC合并3、4指（趾）并指（趾）及多乳头畸形的病例，呈现明显的常染色体显性遗传模式。
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