Diagnosis and Management of Hereditary Hemochromatosis
- 8 November 2022
- journal article
- editorial
- Published by American Medical Association (AMA) in JAMA
- Vol. 328 (18) , 1862-1863
Abstract
This JAMA Insights Clinical Review discusses the diagnosis and management of hereditary hemochromatosis, including clinical and laboratory characteristics, gene testing and interpretation, and the role of imaging and liver biopsy.Keywords
This publication has 9 references indexed in Scilit:
- EASL Clinical Practice Guidelines on haemochromatosisJournal of Hepatology, 2022
- Hereditary Hemochromatosis Rapid Evidence Review2021
- Association of Hemochromatosis HFE p.C282Y Homozygosity With Hepatic MalignancyJAMA, 2020
- Regression of Fibrosis Stage With Treatment Reduces Long-Term Risk of Liver Cancer in Patients With Hemochromatosis Caused by Mutation in HFEClinical Gastroenterology and Hepatology, 2020
- ACG Clinical Guideline: Hereditary HemochromatosisAmerican Journal of Gastroenterology, 2019
- Diagnosis and Management of Genetic Iron Overload DisordersJournal of General Internal Medicine, 2018
- The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosisInternational Journal of Hematology, 2017
- Elevated Serum FerritinJAMA, 2014
- Diagnosis and management of hemochromatosis: 2011 Practice Guideline by the American Association for the Study of Liver DiseasesHepatology, 2011