- dyschromatosis
- An asymptomatic anomaly of pigmentation occurring among the Japanese; may be localized or diffuse. [dys- + G. chroma, color, + -osis, condition]
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dys·chro·ma·to·sis (dis-kro″mə-toґsis) dyschromia.
Medical dictionary. 2011.
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dys·chro·ma·to·sis (dis-kro″mə-toґsis) dyschromia.Medical dictionary. 2011.
Dyschromatosis universalis hereditaria — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD9 = ICDO = OMIM = 127500 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Dyschromatosis universalis hereditaria (DUH) (or Universal dyschromatosis) is a rare genodermatosis … Wikipedia
dyschromatosis symmetrica hereditaria — (DSH) a rare, autosomal dominant pigmentary genodermatosis caused by mutations in the ADAR gene (locus:1q21.3), which encodes adenosine deaminase specific for double stranded RNA, characterized by hyperpigmented and hypopigmented macules that… … Medical dictionary
dyschromatosis universalis hereditaria — (DUH) a rare pigmentary genodermatosis, most often seen in Japan, characterized by hyperpigmented and hypopigmented macules on the trunk, extremities, and sometimes the face that appear in infancy or early childhood. Heredity is autosomal… … Medical dictionary
reticulate acropigmentation of Dohi — dyschromatosis symmetrica hereditaria … Medical dictionary
DUH — dyschromatosis universalis hereditaria … Medical dictionary
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