Dyschromatosis universalis hereditaria with involvement of palms
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چکیده
منابع مشابه
Thrombocytopenia in dyschromatosis universalis hereditaria.
A 14-year old boy presented to causality medical ward with history of left side chest pain and asymptomatic progressive mottled pigmentation over the trunk and limbs, which had been noted since birth and had become more noticeable with age. There was no history of photophobia or photosensitivity. They were born to healthy, non consanguineous parents, following an uneventful pregnancy. His mothe...
متن کاملDyschromatosis Universalis Hereditaria with Renal Failure
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.
متن کاملA 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...
متن کاملRemoval of forearm lentigines in dyschromatosis universalis hereditaria with a 755-nm Q-switched alexandrite laser
DUH: dyschromatosis universalis hereditaria IPL: intense pulsed light INTRODUCTION Characterized by hyperpigmented and hypopigmented macules forming a reticulate pattern, dyschromatosis universalis hereditaria (DUH) was first described by Toyamo in Japan. Subsequent cases have been reported from other areas including Europe, China, Saudi Arabia, Tunisia, India, and Nigeria. A variable autosomal...
متن کاملNovel Mutations of ABCB6 Associated with Autosomal Dominant Dyschromatosis Universalis Hereditaria
OBJECTIVE Dyschromatosis universalis hereditaria (DUH) is a rare heterogeneous pigmentary genodermatosis, which was first described in 1933. The genetic cause has recently been discovered by the discovery of mutations in ABCB6. Here we investigated a Chinese family with typical features of autosomal dominant DUH and 3 unrelated patients with sporadic DUH. METHODS Skin tissues were obtained fr...
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ژورنال
عنوان ژورنال: Indian Dermatology Online Journal
سال: 2014
ISSN: 2229-5178
DOI: 10.4103/2229-5178.137781