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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Int J Surg Case Rep
Egile Nagusiak: Alshomar, Khalid M., Alkatan, Hind M., Alrikabi, Ammar C., Al-Faky, Yasser H.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Elsevier 2021
Gaiak:
Case Report
Sarrera elektronikoa: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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