Dyschromatosis symmetrica hereditaria: A retrospective case series and literature review
Dermatologica Sinica, 2013 Background/Objective: Dyschromatosis symmetrica hereditaria (DSH) is a rare pigmentary genodermatosis characterized by hyper- and hypopigmented macules on the face and dorsal aspects of the extremities.
Sheau-Chiou Chao
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Dyschromatosis symmetrica hereditaria
Journal of Clinical and Scientific ResearchDyschromatosis symmetrica hereditaria (DSH) is an autosomal dominant pigmentary genodermatosis characterised by a mixture of hyperpigmented and hypopigmented macules on the dorsal aspects of the hands and feet.
K. Geetha
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Two Novel and Two Recurrent Variants of the ADAR1 Gene in Three Chinese Families with Dyschromatosis Symmetrica Hereditaria [PDF]
Clinical, Cosmetic and Investigational DermatologyYunxia Zhu,1 Deng Zhang,1 Liang Wu,1 Xiaoliang Ouyang,2 Shengcai Zhu,1 Xiuping Wang,1 Zhen Xiao,3 Yanping Tan,4 Chunming Li1 1Department of Dermatology, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi ...
Zhu Y +8 more
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A rare presentation of dyschromatosis symmetrica hereditaria in a Canadian context: A case report [PDF]
SAGE Open Medical Case ReportsInherited reticulate pigmentary disorders (IRPD) are a group of rare dermatologic conditions characterized by distinct reticulate patterns of hyperpigmentation and/or hypopigmentation of the skin.
Sonia Czyz +2 more
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Identification of the pathogenic variants in three Chinese families with dyschromatosis symmetrica hereditaria [PDF]
Jichu yixue yu linchuang, 2023 Objective To analyze the clinical features and to identify the pathogenic variants in three Chinese families with dyschromatosis symmetrica hereditaria (DSH).
YANG Xueting, GUO Kexin, SUN Yang, WANG Rongrong, MA Donglai, ZHANG Xue
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Analysis of genotype/phenotype correlations in Japanese patients with dyschromatosis symmetrica hereditaria. [PDF]
Nagoya J Med Sci, 2018 Dyschromatosis symmetrica hereditaria (DSH) is one of the genetic pigmentation disorders and shows characteristic mixture of hyper- and hypo-pigmented small macules on the extremities. Heterozygous mutations in the adenosine deaminase acting on RNA1 gene (ADAR1) cause DSH.
Kobayashi T +9 more
europepmc +5 more sources
Dyschromias: A series of five interesting cases from India
Indian Journal of Dermatology, 2015 Dyschromatosis is a pigmentary genodermatosis which presents with hyper and hypopigmented skin lesions giving a mottled appearance. It is a rare entity in India reported mainly in the East Asian population.
Prabhu Namitha, S Sacchidanand
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Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical Manifestations. [PDF]
J DermatolABSTRACT Genetic pigmentary disorders represent a diverse group of genetic conditions characterized by alterations in melanin production and transport and melanocyte development, resulting from single‐gene pathological variants. These disorders encompass both hypopigmentary and hyperpigmentary phenotypes, affecting not only skin pigmentation but also ...
Okamura K, Suzuki T.
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Indian Journal of Dermatology, 2012 Reticulate acropigmentation of Dohi also called dyschromatosis symmetrica hereditaria or symmetrical dyschromatosis of the extremities is an autosomal dominant inherited disorder.
Deepak Mohana +3 more
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A Novel Mutation of the ADAR1 Gene in a Chinese Family with Dyschromatosis Symmetrica Hereditaria and Literature Review [PDF]
Clinical, Cosmetic and Investigational DermatologyHongping Ge,1,2 Na Zhang,1 Xinru Chen,1,3 Meiyan Wang,1 Tianhui Ye1,3 1Department of Dermatology, Jinhua Municipal Central Hospital (Affiliated Jinhua Hospital, Zhejiang University School of Medicine), Jinhua City, Zhejiang Province, People’s Republic of
Ge H, Zhang N, Chen X, Wang M, Ye T
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