Genetic Risk for Hemochromatosis is Associated with Movement Disorders

Published: Aug 24, 2021
Abstract
null Hereditary hemochromatosis (HH) is an autosomal recessive genetic disorder that can lead to iron overload, causing oxidative damage to affected organs. HH type 1 is predominantly associated with homozygosity for the mutation p.C282Y. Previous case studies have reported tentative links between HH and movement disorders, e.g., Parkinson’s disease, and basal ganglia abnormalities on magnetic resonance imaging. We investigated the impact of...
Paper Details
Title
Genetic Risk for Hemochromatosis is Associated with Movement Disorders
Published Date
Aug 24, 2021
Journal
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