Results 61 to 70 of about 434 (146)
Medical Journal of Dr. D.Y. Patil VidyapeethDyschromatosis symmetrica hereditaria (DSH), is an autosomal dominant (AD) genetic disorder with a significant permeation, primarily referred to as reticulate acropigmentation of Dohi.
Banyameen Iqbal +4 more
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Three mutations in SASH1 cause the pathogenesis of dyschromatosis universalis hereditaria (DUH)
, 2011 Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis characterized by hyper- and hypopigmented macules which form a reticulate or mottled pattern.
Zhiyun Wei, Qinghe Xing, Dingan Zhou
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Dyschromatosis universalis hereditaria
Indian Journal of Dermatology, 2009 Dyschromatosis universalis hereditaria is an infrequently occurring genodermatosis with a peculiar pigmentary change, consisting of varying sized hyperpigmented macules mingled with hypopigmented lesions to give an overall impression of mottling.
Naik Chandra +3 more
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Four novel mutations of ADAR1 in Chinese patients with dyschromatosis symmetrica hereditaria
Indian Journal of Dermatology, Venereology and Leprology, 2019 Novel mutations in adenosine deaminase acting on RNA 1 gene (ADAR1) are responsible for dyschromatosis symmetrica hereditaria (DSH). DSH patients display a mixture of hyperpigmented and hypopigmented macules on the dorsal aspects of the extremities, and freckle-like macules on the face.To provide new evidence for further study of the etiopathogenisis ...
Wei, Hu +11 more
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Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of dohi): First report from Iran
Indian Journal of Dermatology, 2009 Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant genodermatosis, presenting in infancy or early childhood with areas of hyperpigmentation on dorsa of hands and feet.
Barzegari Massoumeh, Kiavash Katrin
doaj
Genetics of pigmentary disorders [PDF]
, 2004 The molecular bases of various types of congenital pigmentary disorders have been clarified in the past ten years, as follows. (1) Disorders of melanoblast migration from the neural crest into the skin in embryo (and their disease genes), piebaldism (c ...
Tomita, Yasushi, Suzuki, Tamio
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Dyschromatosis symmetrica hereditaria: Report of a sporadic case in a Nigerian child
Nigerian Journal of PaediatricsDyschromatosissymmetricahereditaria (DSH) is one of a group of reticulate pigment disorders of the skin. It is a rare autosomal dominantly inherited genodermatosis, presenting as mottled admixtures of hypopigmented and hyperpigmented macules on the ...
Henshaw EB, Ntia HU, Archibong JE
doaj
Dyschromatosis Symmetrica Hereditaria (Toyama)
, 1988 departmental bulletin ...
Takahashi, Hidetomo +10 more
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Dyschromatosis symmetrica hereditaria with neurological abnormalities
Indian Journal of Dermatology, Venereology, and Leprology, 2014 SudipKumar Ghosh +2 more
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Dyschromatosis symmetrica hereditaria.
Skin research, 1984 Yokomi, Ikuko +2 more
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