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Article

Association of porphyria cutanea tarda with hereditary hemochromatosis.

Journal of the American Academy of Dermatology - 1 Aug 2004

Mehrany Khosrow, Drage Lisa A, Brandhagen David J, Pittelkow Mark R

Abstract excerpt

BACKGROUND: An increased frequency of hereditary hemochromatosis gene mutations occurs in patients with porphyria cutanea tarda. Polymerase chain reaction analysis of peripheral blood for hemochromatosis gene (HFE) mutations is available for clinical use. Early detection and treatment of heredita...

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Source

Identifiers

PMID: 15280838
DOI: 10.1016/j.jaad.2003.08.015

Genes

HFE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15280838-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Association of porphyria cutanea tarda with hereditary hemochromatosis.PMID 15280838Read ↗

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C282Y and H63D mutation of the hemochromatosis gene in German porphyria cutanea tarda patients.Semantic proximity Read ↗

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The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients.Semantic proximity Read ↗

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Hemochromatosis (HFE) gene mutations and hepatitis C virus infection as risk factors for porphyria cutanea tarda in Hungarian patients.Semantic proximity Read ↗

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