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A Rare Case of Hereditary Hemochromatosis Presenting With Porphyria Cutanea Tarda
Hereditary hemochromatosis is an autosomal recessive condition with incomplete penetrance that is most commonly caused by a mutation in the HFE gene. Hereditary hemochromatosis can remain asymptomatic in some patients until triggered by certain events. Porphyria cutanea tarda is a condition that can...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394580/ https://www.ncbi.nlm.nih.gov/pubmed/37539416 http://dx.doi.org/10.7759/cureus.41299 |