Evolution of the skin manifestations of X-linked pigmentary reticulate disorder.
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ABSTRACT:
SUBMITTER: Starokadomskyy P
PROVIDER: S-EPMC5640471 | biostudies-literature | 2017 Nov
REPOSITORIES: biostudies-literature
Publications
Evolution of the skin manifestations of X-linked pigmentary reticulate disorder.
Starokadomskyy P P Sifuentes-Dominguez L L Gemelli T T Zinn A R AR Dossi M T MT Mellado C C Bertrand P P Borzutzky A A Burstein E E
The British journal of dermatology 20171008 5
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Project description:Reticulate pigmentary disorders (RPDs) are a group of inherited and acquired skin conditions characterized by hyperpigmented and/or hypopigmented macules. Inherited RPDs include dyschromatosis symmetrica hereditaria (DSH), dyschromatosis universalis hereditaria (DUH), reticulate acropigmentation of Kitamura (RAK), Dowling-Degos disease (DDD), dyskeratosis congenita (DKC), Naegeli-Franceschetti-Jadassohn syndrome (NFJS), dermatopathia pigmentosa reticularis (DPR), and X-linked reticulate pigmentary disorder. Although reticulate pattern of pigmentation is a common characteristic of this spectrum of disorders, the distribution of pigmentation varies among these disorders, and there may be clinical manifestations beyond pigmentation. DSH, DUH, and RAK are mostly reported in East Asian ethnicities. DDD is more common in Caucasians, although it is also reported in Asian countries. Other RPDs show no racial predilection. This article reviews the clinical, histological, and genetic variations of inherited RPDs.
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