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Article

Dyschromatosis symmetrica hereditaria associated with neurological disorders.

The Journal of dermatology - 1 Oct 2008

Kondo Taisuke, Suzuki Tamio, Ito Shiro, Kono Michihiro, Negoro Tamiko, Tomita Yasushi

Abstract excerpt

Dyschromatosis symmetrica hereditaria (DSH) is a pigmentary genodermatosis of autosomal dominant inheritance caused by a mutation of adenosine deaminase acting on the RNA 1 gene (ADAR1). It is characterized by a mixture of hyper- and hypopigmented macules on the back of the hands and feet. The pathomechanism by which the ADAR1 gene mutation induces DSH has not been clarified yet. We experienced an 11-year-old...

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Identifiers

PMID: 19017046
DOI: 10.1111/j.1346-8138.2008.00540.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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