dyschromatosis

dys·chro·ma·to·sis

(dis'krō-mă-tō'sis),
An asymptomatic anomaly of pigmentation occurring among the Japanese; may be localized or diffuse.
[dys- + G. chrōma, color, + -osis, condition]
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References in periodicals archive ?
It comprises of a spectrum of diseases which include dyschromatosis universalis hereditaria (DUH) or acropigmentation of Dohi and segmental form called unilateral dermatomal pigmentary dermatosis (UDPD).
The differential diagnoses of generalized RPD are dyschromatosis universalis hereditaria (DUH), dermatopathia pigmentosa reticularis (DPR), Naegeli- Franceschetti-Jadassohn syndrome and dyskeratosis congenita (DKC).
Dyschromatosis universalis hereditaria: report of a case and review of the literature.
Universal dyschromatosis, small stature and high tone deafness.
Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria.
Dyschromatosis universalis hereditaria (DUH) and dyschromatosis symmetrica hereditaria are two major types.
sup][1] Dyschromatosis universalis hereditaria (DUH; Online Mendelian Inheritance in Man [OMIM] 127500, 615402 and 612715) and dyschromatosis symmetrica hereditaria (DSH; OMIM 127400) are two classic forms of dyschromatoses.
Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): Report of a Japanese family with the condition and a literature review of 185 cases.
Dyschromatosis universalis hereditaria: Evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23.
Mutations in ABCB6 cause dyschromatosis universalis hereditaria.
There is an increase in the number of mitoses, and dyskaryosis, anisokaryosis, and dyschromatosis are present (figure 3).
Besides ACD, there are many other diseases with the characteristics of cutaneous dyschromia, includes dyschromatosis universalis hereditaria, xeroderma pigmentosum and poikiloderma-like amyloidosis.