JAAD Case Reports (Aug 2024)

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

  • Jonathan Banta, MD,
  • Joshua Collins, DO,
  • Todd Kobayashi, MD

Journal volume & issue
Vol. 50
pp. 30 – 32

Abstract

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Keywords