Dyschromatosis Universalis Hereditaria - Case Report of a Rare Genodermatosis in India
نویسندگان
چکیده
منابع مشابه
A Case of Sporadic Dyschromatosis Universalis Hereditaria
Vol. 27, No. 4, 2015 467 Received July 21, 2014, Revised August 25, 2014, Accepted for publication September 1, 2014 Corresponding author: Kyu Uang Whang, Department of Dermatology, Soonchunhyang University Seoul Hospital, 59 Daesagwan-ro, Yongsan-gu, Seoul 140-743, Korea. Tel: 82-2-709-9368, Fax: 82-2709-9139, E-mail: [email protected] This is an Open Access article distributed under the te...
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Dyschromatosis universalis hereditaria (DUH) is a rare autosomal dominant inherited dermatosis which usually appears during childhood and is characterized by dyspigmentation, with both hypopigmented and hyperpigmented macules. We report a case of DUH with unexplained childhood-onset renal failure. The association between DUH and renal failure is yet to be proven by further studies.
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متن کاملDowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family.
Dowling-Degos disease is a rare autosomal dominant inherited pigmentary disorder characterized by reticulate pigmentation of the flexures, prominent comedone like lesions and pitted scars. Dyschromatosis universalis hereditaria is characterized by the presence of hypopigmented as well as hyperpigmented macules. We report a family showing features of both these diseases.
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ژورنال
عنوان ژورنال: Annals of International medical and Dental Research
سال: 2017
ISSN: 2395-2814,2395-2822
DOI: 10.21276/aimdr.2017.3.2.pe4