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1. 色素沈着不全 the dyschromatoses
2. 先天性や遺伝性の色素増加症 congenital and inherited hyperpigmentation disorders

English Journal

Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.

Suzuki N1, Suzuki T, Inagaki K, Ito S, Kono M, Fukai K, Takama H, Sato K, Ishikawa O, Abe M, Shimizu H, Kawai M, Horikawa T, Yoshida K, Matsumoto K, Terui T, Tsujioka K, Tomita Y.
The Journal of investigative dermatology.J Invest Dermatol.2005 Jun;124(6):1186-92.
PMID 15955093

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