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

Internet

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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