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A rare case of porphyria cutanea tarda in a patient with a homozygous hereditary hemochromatosis gene H63D mutation in the setting of hereditary hemochromatosis

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Main Authors: Jonathan Banta, MD, Joshua Collins, DO, Todd Kobayashi, MD
Format: Artigo
Language:Inglês
Published: Elsevier 2024-08-01
Series:JAAD Case Reports
Subjects:
hereditary hemochromatosis
liver
porphyria cutanea tarda
skin
Online Access:http://www.sciencedirect.com/science/article/pii/S2352512624002042
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