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北村网状肢端色素沉着症的遗传方式总是常染色体显性遗传吗?

Is the heredity of reticulate acro pigmentation of Kitamura always autosomal dominant?

作者信息

Singal A, Bhattacharya S N, Baruah M C, Indrayan A, Singh N

机构信息

Department of Dermatology & STD, University College of Medical Sciences, Delhi, India.

出版信息

J Dermatol. 1998 Jan;25(1):57-9. doi: 10.1111/j.1346-8138.1998.tb02348.x.

Abstract

Reticulate acropigmentation of Kitamura (RAK) in three patients and their families is described. In one family, 2 women and 2 men were affected out of 9 individuals. In the other family, 6 women had lesions of reticulate acropigmentation out of total of 27 over three generations. In the third family, one man was affected. All of the cases had palmar pits; onset of lesions was after puberty in all the cases. The apparently different hereditary patterns in these three families are striking, and autosomal dominant inheritance appears unlikely in every case.

摘要

本文描述了三例木村网状肢端色素沉着症(RAK)患者及其家族情况。在一个家族中,9名成员中有2名女性和2名男性患病。在另一个家族中,三代共27名成员中有6名女性患有网状肢端色素沉着症。在第三个家族中,有一名男性患病。所有病例均有掌部凹点;所有病例的皮损均在青春期后出现。这三个家族明显不同的遗传模式令人瞩目,且在每个病例中常染色体显性遗传似乎都不太可能。

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