遗传性泛发性色素异常症：来自一个家族的6例报告
Dyschromatosis universalis hereditaria: report of six cases from a family.
作者信息
Sardar Swapan Kumar, Das Anupam, Bandyopadhyay Debabrata Bandyopadhyay
机构信息
Department of Dermatology, KPC Medical College and Hospital, Kolkata.
出版信息
Dermatol Online J. 2016 Sep 15;22(9):13030/qt24p9j62b.
Dyschromatosis universalis hereditaria (DUH) is a rare pigmentary disorder characterized by the presence of mottled hyperpigmented and hypopigmented macules over the trunk, extremities, and face. We have presented a case series comprised of six members of a family who had numerous hyperpigmented and hypopigmented macules distributed all over the body. Histological findings were suggestive of dyschromatosis universalis hereditaria.
遗传性泛发性色素异常症（DUH）是一种罕见的色素沉着障碍性疾病，其特征为躯干、四肢和面部出现斑驳的色素沉着过度和色素沉着不足的斑疹。我们报告了一个家系的6名成员，他们全身有大量色素沉着过度和色素沉着不足的斑疹。组织学检查结果提示为遗传性泛发性色素异常症。
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