Diagnosis and Management of Hereditary Hemochromatosis
Date Added:
November 12, 2022
Journal/Publication:
JAMA
Publisher:
Massachusetts Medical Society
Publication Date:
November 8, 2022
Issue:
18
Volume:
328
Pages:
1862-1863
Type:
Meta-analyses, Reviews, and Guidelines
Format:
Article
DOI (1):
10.1001/jama.2022.17727
PMID (1):
36346422
Abstract
Hereditary hemochromatosis (HH) is a heterogeneous genetic disorder that results in unregulated and excessive intestinal iron absorption leading to overabundance of iron deposition in tissue. HH is most common in people of northern European ancestry, for whom the prevalence is 1 case per 300 people.1-3
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RPR Commentary
A updated summary of the pathophysiology, diagnosis, and treatment of hemochromatosis. James W. Mold, MD, MPH