WebDyschromatosis symmetrica hereditaria 1 is a genetic disease, which means that it is caused by one or more genes not working correctly. Disease-causing variants, or … WebSelect search scope, currently: articles+ all catalog, articles, website, & more in one search; catalog books, media & more in the Stanford Libraries' collections; articles+ journal articles & other e-resources
Dyschromatosis symmetrica hereditaria - Wikipedia
Dyschromatosis symmetrica hereditaria (also known as "reticulate acropigmentation of Dohi", and "symmetrical dyschromatosis of the extremities") is a rare autosomally inherited dermatosis. It is characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities. It presents primarily in the Japanese, b… WebNov 10, 2011 · Dyschromatosis symmetrica hereditaria (DSH, also known as acropigmentation of Dohi) is an autosomal dominant genodermatosis, characterized by multiple small hypo- and hyperpigmented macules of irregular size and shape, distributed symmetrically on the face and distal limbs, especially the dorsa of the hands and feet . … greenhouse lean to uk
Entry - #127500 - DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1; DUH1 …
WebMar 1, 2013 · Dyschromatosis symmetrica hereditaria (DSH) is a rare pigmentary genodermatosis characterized by hyper- and hypopigmented macules on the face … WebMore than 180 ADAR gene mutations have been identified in people with dyschromatosis symmetrica hereditaria. This disorder is characterized by freckle-like spots (macules) … WebIt is a spectrum of diseases, which includes DUH, dyschromatosis symmetrica hereditaria (DSH) or acropigmentation of Dohi, and a segmental form called unilateral dermatomal pigmentary dermatosis. In 1929, Toyama described DSH as a distinct entity, later in 1933, Ichikawa and Hiraga described DUH, which had similar features of DSH … greenhouse learning bristol