A Case Report of Dyschromatosis Symmetrica Hereditaria with Glucose-6-Phosphate Dehydrogenase Deficiency

被引：0
|
作者：
Wang, Panpan [1 ]
Tang, Chenyu [1 ]
Zhao, Yige [1 ]
Wang, Ping [2 ]
机构：
[1] Zhejiang Chinese Med Univ, Hangzhou Peoples Hosp 3, Dept Dermatol, Hangzhou, Peoples R China
[2] Zhejiang Univ, Hangzhou Peoples Hosp 3, Dept Dermatol, Hangzhou Dermatol Hosp,Sch Med, Westlake Ave 38, Hangzhou, Peoples R China
来源：
CLINICAL COSMETIC AND INVESTIGATIONAL DERMATOLOGY | 2023年 / 16卷
关键词：
dyschromatosis symmetrica hereditaria; glucose-6-phosphate dehydrogenase deficiency; psychosis; ADAR1; MUTATIONS; GENE;
D O I：
10.2147/CCID.S407052
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
Dyschromatosis symmetrica hereditaria (DSH) is a pigmented genetic skin disorder with an incompletely understood pathogenesis characterized by reticular hyper-and hypopigmented skin patches on the dorsal aspect of the extremities, freckle-like patches on the face, and unaffected palms and feet. There is no effective treatment available. Glucose-6-phosphate dehydrogenase (G6PD) deficiency has not been reported in the literature of DSH. We describe for the first time a case of DSH with G6PD deficiency and a family history of psychosis.
引用
收藏
页码：1047 / 1050
页数：4
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