遗传性少毛症与局限性硬皮病：一种新的临床实体。
Hereditary hypotrichosis and localized morphea: a new clinical entity.
作者信息
Kulin P, Sybert V P
出版信息
Pediatr Dermatol. 1986 Sep;3(4):333-8. doi: 10.1111/j.1525-1470.1986.tb00536.x.
Abstract
A family with childhood onset of hypotrichosis and morphea with apparent autosomal dominant inheritance is reported. Careful literature review suggests that this is a previously undescribed disorder.
摘要
报告了一个具有常染色体显性遗传特征、童年期发病的毛发稀少症和硬斑病家族。仔细的文献回顾表明，这是一种此前未被描述的疾病。
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