遗传性全身性色素异常伴尿道下裂：一种罕见的关联。
Dyschromatosis Universalis Hereditaria with Hypospadias: A Rare Association.
作者信息
Sirka Chandra Sekhar, Sahu Kananbala, Rout Arpita Nibedita
机构信息
Department of Dermatology, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.
出版信息
Indian Dermatol Online J. 2020 Mar 9;11(2):243-245. doi: 10.4103/idoj.IDOJ_143_19. eCollection 2020 Mar-Apr.
Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis, which presents as hyper- and hypopigmented macules all over the body. Although a benign condition, rarely DUH is associated with abnormalities of dermal connective tissue, nerve, and systemic conditions. We report a case of DUH associated hypospadias and complicated with hydronephrosis that has not been described earlier.
遗传性泛发性色素异常症（DUH）是一种罕见的遗传性皮肤病，表现为全身出现色素沉着过多和色素沉着过少的斑疹。尽管是良性疾病，但DUH很少与真皮结缔组织、神经异常及全身疾病相关。我们报告一例DUH合并尿道下裂并并发肾积水的病例，此前未见相关报道。
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