Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria
نویسندگان
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 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...
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: Indian Journal of Dermatology, Venereology and Leprology
سال: 2006
ISSN: 0378-6323
DOI: 10.4103/0378-6323.26729