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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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| Publicado no: | Int J Surg Case Rep |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7809158/ https://ncbi.nlm.nih.gov/pubmed/33434773 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijscr.2021.01.012 |
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