Aceruloplasminemia Clinical signs and pathophysiological mechanisms

By EMNA ELLOUZ and Imen Ketata

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

• Format: Paperback
• Language: English
• ISBN: 6207624343
• ISBN13: 9786207624348
• Release Date: June 2024
• Publisher: Our Knowledge Publishing
• Length: 72 Pages
• Weight: 0.26 lbs.
• Dimensions: 0.2" x 6.0" x 9.0"