A Rare Case of Hereditary Hemochromatosis Presenting With Porphyria Cutanea Tarda

Author:

Varada Neilmegh,Tun Kyaw Min,Chang Mark J,Bomberger Shana,Calagari Randy

Publisher

Springer Science and Business Media LLC

Subject

Aerospace Engineering

Reference6 articles.

1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder JN;Nat Genet,1996

2. Iron as a co-morbid factor in nonhemochromatotic liver disease;Bonkovsky HL;Alcohol,2003

3. Association of porphyria cutanea tarda with hereditary hemochromatosis;Mehrany K;J Am Acad Dermatol,2004

4. Early presentation of adult-onset conditions: a dual diagnosis of hereditary hemochromatosis and porphyria cutanea tarda;Strong A;Mol Genet Metab Rep,2020

5. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers;Melis MA;Haematologica,2002

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