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...
Saved in:
Main Authors: | Fatima Mendonca Jorge Vieira (Author), Maria Cristina Nakhle (Author), Clarice Pires Abrantes-Lemos (Author), Eduardo Luiz Rachid Cancado (Author), Vitor Manoel Silva dos Reis (Author) |
---|---|
Format: | Book |
Published: |
Sociedade Brasileira de Dermatologia,
2013-08-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Porfiria cutânea tardia Porphyria cutanea tarda
by: Fátima Mendonça Jorge Vieira, et al.
Published: (2006) -
Pregnancy Induced Porphyria Cutanea Tarda
by: Shanker B, et al.
Published: (2000) -
Porphyria cutanea tarda and Sjogren's syndrome
by: Su Fang, et al.
Published: (2014) -
Porphyria cutanea tarda associated with HFE C282Y homozygosity, iron overload, and use of a contraceptive vaginal ring
by: James C. Barton, et al.
Published: (2016) -
Atypical porphyria cutanea tarda mimicking morphea
by: Maria J. Guimarães, et al.
Published: (2023)