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Identification of two novel mutations in Chinese patients with Dyschromatosis symmetrica hereditaria.

Archives of dermatological research - 1 Nov 2005

Li Ming, Li Chengrang, Hua Haikang, Zhu Wenyuan, Lu Yan, Yang Lijia

Abstract excerpt

Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant cutaneous disorder characterized by a mixture of hyperpigmented and hypopigmented macules of various sizes on the extremities. Pathogenic mutations in the DSRAD gene have recently been identified. In this study, we report an...

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PMID: 16215765
DOI: 10.1007/s00403-005-0595-3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16215765-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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