Results 141 to 150 of about 695 (177)

Dermoscopy of Familial Gigantic Melanocytosis: A Report of Rare Entity.

Indian J Dermatol
Ankad BS, Nikam BP, Chigurupati E.
europepmc   +1 more source

Acquired brachial cutaneous dyschromatosis

Clinics in Dermatology, 2021
Acquired brachial cutaneous dyschromatosis (ABCD) is a relatively newly described, acquired disorder of pigmentation characterized by geographic-shaped, gray-brown, hyperpigmented patches and interspersed with hypopigmented macules, involving the dorsal aspects of the forearms in postmenopausal women. There is a suggested relationship with hypertension
Rongioletti F., Atzori L., Ferreli C.
openaire   +4 more sources

Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation

American Journal of Medical Genetics, Part A, 2004
We report a familial case of dyschromatosis universalis hereditaria (DUH) which is compatible with an autosomal dominant inheritance. The male proband from Bangladesh presented with randomly distributed hyper- and hypo-pigmented skin lesions of variable ...
Stefan Mundlos
exaly   +3 more sources

Identification of a Locus for Dyschromatosis Symmetrica Hereditaria at Chromosome 1q11–1q21

Journal of Investigative Dermatology, 2003
Dyschromatosis symmetrica hereditaria is a rare autosomal dominant cutaneous disorder characterized by a mixture of hyperpigmented and hypopigmented macules of various sizes on the face and the dorsal aspects of the extremities.
Ping-Ping He, Shi-Jie Xu, Zai-Xing Wang   +2 more
exaly   +2 more sources

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Dyschromatosis universalis hereditaria

International Journal of Dermatology, 2023
AbstractReticulate pigmentary dyschromatoses primarily include dyschromatosis universalis hereditaria (DUH), dyschromatosis symmetrica hereditaria (DSH) (Reticulate acropigmentation of Dohi), and unilateral dermatomal pigmentary dermatosis, which differ in their patterns of distribution.
Aravind B. Murthy, Vijayasankar Palaniappan, Kaliaperumal Karthikeyan, Varshini Anbarasan   +3 more
openaire   +2 more sources

Novel Mutations of the RNA-Specific Adenosine Deaminase Gene (DSRAD) in Chinese Families with Dyschromatosis Symmetrica Hereditaria

Journal of Investigative Dermatology, 2004
Dyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant skin disorder. It is also called “reticulate acropigmentation of Dohi” or “symmetric dyschromatosis of the extremities”.
Qing Liu, Xiuli Zhao
exaly   +2 more sources

Dyschromatosis

Seminars in Cutaneous Medicine and Surgery, 1997
The dyschromatoses are a group of disorders characterized by the presence of both hyperpigmented and hypopigmented macules, many of which are small in size and irregular in shape. There are two major forms-dyschromatosis symmetrica hereditaria (DSH) and dyschromatosis universalis hereditaria (DUH), both of which are seen most commonly in Japan. DSH was
K, Urabe, Y, Hori
openaire   +2 more sources

Dyschromatosis symmetrica hereditaria

The Journal of Dermatology, 2012
ABSTRACTDyschromatosis symmetrica hereditaria (DSH) is a rare pigmentary genodermatosis, which is acquired by autosomal dominant inheritance with high penetrance. Most cases of this condition have been reported from East Asian countries, including Japan, China and Taiwan.
Masahiro, Hayashi, Tamio, Suzuki
openaire   +2 more sources

Dyschromatosis universalis hereditaria

Clinical and Experimental Dermatology, 2002
Dyschromatosis universalis hereditaria is a clinically heterogenous disorder. We report two unrelated Indian patients with dyschromatosis universalis hereditaria, who had generalized and progressive reticulate hyper- and hypo-pigmentation of the skin. The oral mucosa and tongue also showed mottled pigmentation.
G. Sethuraman, M. D'Souza, D. Mohan Thappa, C. R. Srinivas, L. Smiles   +4 more
openaire   +2 more sources

Dyschromatosis

, 2019
Liat Samuelov, Eli Sprecher
exaly   +2 more sources