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Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios

Later, it may present with phenotypic abnormalities resembling Marfan syndrome, osteoporosis, ectopia lentis, and recurrent thrombosis

Therapeutic strategies simultaneously targeting -syn aggregation and ferroptosis pathways hold promise for modifying disease progression

This article explains the benefits and reviews specific case studies involving chiropractic care for children with ADHD and sensory learning disorders (50)

10.1186/s12967-017-1345-y 99

If you or a loved one have suffered injuries, property damage, or other financial losses due to a truck accident in St