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...

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Detalles Bibliográficos
Autores principales: Varada, Neilmegh, Tun, Kyaw Min, Chang, Mark J, Bomberger, Shana, Calagari, Randy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Internal Medicine
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

Internet

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

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