Abstract
First described in 1929, dyschromatosis universalis hereditaria (DUH) occurred mostly in Asia. Though its uncertainty mode of inheritance, patients affected with this disease showed asymptomatic hypo- and hyper-pigmented macules of irregular size and shape involving almost the whole of the body. Face, palm and sole can be affected. Here we report a case from China, and cases reported from 1977 were reviewed.
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References
Imamura S. Skin diseases first described in Japan. Clin Dermatol. 1999;17(2):117–26.
Al Hawsawi K, et al. Dyschromatosis universalis hereditaria: report of a case and review of the literature. Pediatr Dermatol. 2002;19(6):523–9.
Nan W, Tang L, Li X, Dai Y, Zheng X, Gao M, Wang P. Identification of a novel mutation in SASH1 gene in a Chinese family with Dyschromatosis Universalis Hereditaria and genotype-phenotype correlation analysis. Front Genet. 2020;4(11):841.
Zhong W, Pan Y, Shao Y, Yang Y, Yu B, Lin Z. Atypical presentation of dyschromatosis universalis hereditaria with a novel ABCB6 mutation. Clin Exp Dermatol. 2019;44(3):e58–60.
Alshaikh H, Alsaif F, Aldukhi S. Clinical and genetic review of hereditary acral reticulate pigmentary disorders. Dermatol Res Pract. 2017;2017:3518568.
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An, J., Geng, S. (2022). A Young Boy with Hyperpigmented and Hypopigmented Macules. In: Lotti, T.M., Arcangeli, F. (eds) Clinical Cases in Adolescent Dermatology. Clinical Cases in Dermatology. Springer, Cham. https://doi.org/10.1007/978-3-030-91526-1_7
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DOI: https://doi.org/10.1007/978-3-030-91526-1_7
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