Aceruloplasminemia Clinical signs and pathophysiological mechanisms
English


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About The Book

Aceruloplasminemia a rare genetic disease is characterized by a variety of clinical symptoms and tissue iron accumulation with the underlying mechanisms largely unknown. Our meta-analysis of 110 patients performed according to PRISMA 2020 guidelines revealed that males with ferritin levels >700 ng/ml start the disease with diabetes while females or those with ferritin
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