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遗传性对称性色素沉着症伴 6- 磷酸葡萄糖脱氢酶缺乏症一例报告
Authors Wang P, Tang C, Zhao Y, Wang P
Received 17 February 2023
Accepted for publication 4 April 2023
Published 19 April 2023 Volume 2023:16 Pages 1047—1050
DOI https://doi.org/10.2147/CCID.S407052
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Jeffrey Weinberg
Abstract: 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.
Keywords: dyschromatosis symmetrica hereditaria, glucose-6-phosphate dehydrogenase deficiency, psychosis, ADAR1