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Juvenile Hemochromatosis: A Case Report and Review of the Literature

Juvenile hemochromatosis (JH), type 2A hemochromatosis, is a rare autosomal recessive disorder of systemic iron overload due to homozygous mutations of HJV (HFE2), which encodes hemojuvelin, an essential regulator of the hepcidin expression, causing liver fibrosis, diabetes, and heart failure before...

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Detalles Bibliográficos
Autores principales:	Takami, Akiyoshi, Tatsumi, Yasuaki, Sakai, Katsuhisa, Toki, Yasumichi, Ikuta, Katsuya, Oohigashi, Yuka, Takagi, Junko, Kato, Koichi, Takami, Kazuhisa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465211/ https://www.ncbi.nlm.nih.gov/pubmed/32824233 http://dx.doi.org/10.3390/ph13080195

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