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Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype

Subnetwork: Haemochromatosis and other iron disorders

Disease group/s: HFE-related hereditary hemochromatosis with established severe clinical expression or due to very rare mutations in HFE

Scope and Purpose: 3. Treatment

Patients' involvement?: Yes

Rigour of development: C - Expert opinion

Link: https://www.ncbi.nlm.nih.gov/pubmed/29589198