一例遗传性泛发性色素异常症合并无指纹症：一种罕见的关联。
A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association.
作者信息
Kumar Sumir, Bhoyar Pritish, Mahajan Bharat Bhushan
机构信息
Department of Skin and VD, Guru Gobind Singh Medical College, Faridkot, Punjab, India.
出版信息
Indian Dermatol Online J. 2015 Mar-Apr;6(2):105-9. doi: 10.4103/2229-5178.153013.
Abstract
Dyschromatosis universalis hereditaria (DUH) is a rare, autosomal dominant genodermatosis with a peculiar reticulate pigmentary change, consisting of hyperpigmented macules mingled with hypopigmented lesions to give an overall impression of mottling. We herein report a case of DUH with adermatoglyphia in a young male with family history of the disorder.
摘要
遗传性泛发性色素异常症（DUH）是一种罕见的常染色体显性遗传性皮肤病，具有独特的网状色素变化，由色素沉着斑与色素减退性损害混合而成，整体呈现出斑驳的外观。我们在此报告一例患有无指纹症的DUH病例，该患者为一名年轻男性，有该疾病的家族史。
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