Precipitating factors of porphyria cutanea tarda in Brazil with emphasis on hemochromatosis gene (HFE) mutations. Study of 60 patients*

BACKGROUND: Porphyria cutanea tarda is the most common form of porphyria, characterized by the decreased activity of the uroporphyrinogen decarboxylase enzyme. Several reports associated HFE gene mutations of hereditary hemochromatosis with porphyria cutanea tarda worldwide, although up to date only...

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Hlavní autoři: Vieira, Fatima Mendonça Jorge, Nakhle, Maria Cristina, Abrantes-Lemos, Clarice Pires, Cançado, Eduardo Luiz Rachid, dos Reis, Vitor Manoel Silva
Médium: Artigo
Jazyk:Inglês
Vydáno: Sociedade Brasileira de Dermatologia 2013
Témata:
Investigation
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3760927/
https://ncbi.nlm.nih.gov/pubmed/24068123
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20132048
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