A rare case of porphyria cutanea tarda in a patient with a homozygous hereditary hemochromatosis gene H63D mutation in the setting of hereditary hemochromatosis-Reference-Cited by-同舟云学术

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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

Published:2024-08 Issue: Volume:50 Page:30-32
ISSN:2352-5126
Container-title:JAAD Case Reports
language:en
Short-container-title:JAAD Case Reports

Author:

Banta Jonathan,Collins Joshua,Kobayashi Todd

Publisher

Elsevier BV

Reference10 articles.

1. Increased mortality in patients with porphyria cutanea tarda-A nationwide cohort study;Christiansen;J Am Acad Dermatol,2020

2. Porphyria cutanea tarda--when skin meets liver;Frank;Best Pract Res Clin Gastroenterol,2010

3. Porphyria cutanea tarda, hepatitis C, uroporphyrinogen decarboxylase and mutations of HFE gene. A case-control study;Cribier;Dermatology,2009

4. Hemochromatosis gene sequence deviations in German patients with porphyria cutanea tarda;Frank;Physiol Res,2006

5. Hereditary hemochromatosis presenting as porphyria cutanea tarda in a patient homozygous for the HFE H63D mutation;Kraft;J Am Acad Dermatol,2007

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