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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Detaylı Bibliyografya
Yayımlandı:Pharmaceuticals (Basel)
Asıl Yazarlar: Takami, Akiyoshi, Tatsumi, Yasuaki, Sakai, Katsuhisa, Toki, Yasumichi, Ikuta, Katsuya, Oohigashi, Yuka, Takagi, Junko, Kato, Koichi, Takami, Kazuhisa
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2020
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7465211/
https://ncbi.nlm.nih.gov/pubmed/32824233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ph13080195
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