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A case of dyschromatosis symmetrica hereditaria with an associated eyelid hemangioma

INTRODUCTION AND IMPORTANCE: Dyschromatosis symmetrica hereditaria (DSH) are rare autosomal dominant pigmentary genodermatosis characterized by reticular hyper- and hypopigmented skin macules on the dorsal aspect of the extremities and freckle-like spots on the face, sparing the palms and soles. Cut...

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Detalles Bibliográficos
Autores principales:	Alshomar, Khalid M., Alkatan, Hind M., Alrikabi, Ammar C., Al-Faky, Yasser H.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809158/ https://www.ncbi.nlm.nih.gov/pubmed/33434773 http://dx.doi.org/10.1016/j.ijscr.2021.01.012

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