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・ Dysgonia torrida
・ Dyschirius vanhillei
・ Dyschirius varidens
・ Dyschirius verticalis
・ Dyschirius vietnamicus
・ Dyschirius wayah
・ Dyschirius weyrauchi
・ Dyschirius yezoensis
・ Dyschirius zambesiensis
・ Dyschirius zanzibaricus
・ Dyschirius zimini
・ Dyschlorodes
・ Dyschloropsis
・ Dyschoriste
・ Dyschoroneura
Dyschromatosis symmetrica hereditaria
・ Dyschromatosis universalis hereditaria
・ Dyschromia
・ Dyschronometria
・ Dyscia
・ Dyscia atlantica
・ Dyscia conspersaria
・ Dyscia fagaria
・ Dyscinetonyssus
・ Dyscolus
・ Dyscophellus
・ Dyscophus antongilii
・ Dyscophus guineti
・ Dyscophus insularis
・ Dyscopia


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Dyschromatosis symmetrica hereditaria : ウィキペディア英語版
Dyschromatosis symmetrica hereditaria
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.〔James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.〕 It presents primarily in the Japanese, but has also been found to affect individuals from Europe, India and the Caribbean.
==Genetics==

This disease is caused by mutation in the double stranded RNA specific adenosine deaminase (ADAR1) gene.〔Zhang GL, Shi HJ, Shao MH, Li M, Mu HJ, Gu Y, Du XF, Xie P (2013) Mutations in the ADAR1 gene in 2 Chinese families with dyschromatosis symmetrica hereditaria. Genet Mol Res 12(AOP)〕 This gene is located on the long arm of chromosome 1 (1q21)

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