A novel missense mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria

Auteur(s) : Yingying Dong1, Shengxiang Xiao1, Jianwen Ren1, Jia Huo1, Yan Liu1, Xiaoli Li1 Department of Dermatology, Second Hospital of Xi’an Jiaotong University, 157 Xi Wu Road, Xi’an, Shaanxi, 710004, China Dyschromatosis symmetrica hereditaria (DSH; MIM127400) is an autosomal dominant skin disorder characterized by a mixture of hyperpigmented and hypopigmented macules of various sizes on the back of the hands and feet. Many patients with DSH also have small freckle-like pigmented [...]