家族性反应性穿通性胶原病：一例报告。

Familial reactive perforating collagenosis: a case report.

作者信息

Kumar V, Mehndiratta V, Sharma R C, Narayan S, Koranne R V, Kakar N

机构信息

Department of Dermatology, Lady Hardinge Medical College, New Delhi, India.

出版信息

J Dermatol. 1998 Jan;25(1):54-6. doi: 10.1111/j.1346-8138.1998.tb02347.x.

DOI:10.1111/j.1346-8138.1998.tb02347.x

PMID:9519612

Abstract

Reactive perforating collagenosis is characterised by trans-epidermal elimination of collagen and is hypothesized to be both autosomally dominant and recessive. We report a family in which two brothers and a sister had lesions of reactive perforating collagenosis.

摘要

反应性穿通性胶原病的特征是胶原蛋白经表皮排出，据推测其遗传方式为常染色体显性和隐性。我们报告了一个家族，其中两兄弟和一个姐妹患有反应性穿通性胶原病。