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PMID: 15464654 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Pathogenesis of hereditary hemochromatosis.

Clinics in liver disease ·Vol. 8 ·No. 4 ·2004-11-00 ·Pages 755-73, vii

Fleming RE, Britton RS, Waheed A, Sly WS, Bacon BR

Abstract

Hereditary hemochromatosis comprises several inherited disorders of iron homeostasis characterized by increased gastrointestinal iron absorpstion and resultant tissue iron deposition. The identification of HFE and other genes involved in iron metabolism has greatly expanded our understanding of hereditary hemochromatosis. Two major hypotheses have been proposed to explain the pathogenesis of HFE-related hereditary hemochromatosis: the hepcidin hypothesis and the duodenal crypt cell programming hypothesis.

MeSH Terms
Animals Antimicrobial Cationic Peptides/pharmacology Disease Models, Animal Duodenum/cytology,physiology Genetic Predisposition to Disease Hemochromatosis/genetics,physiopathology Hepcidins Humans Iron/metabolism,pharmacokinetics Mice
Chemicals
Antimicrobial Cationic Peptides HAMP protein, human Hamp protein, mouse Hepcidins Iron
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Fleming Robert E
Department of Pediatrics, Saint Louis University School of Medicine, Cardinal Glennon Childrens Hospital, 1465 S. Grand Blvd, St. Louis, MO 63104, USA. flemingr@slu.edu
Britton Robert S
Waheed Abdul
Sly William S
Bacon Bruce R
Article Info
Journal
Clinics in liver disease
Abbr.
Clin Liver Dis
ISSN
1089-3261
Published
2004-11-00
Pages
755-73, vii
Language
English
Region
United States
NLM ID
9710002
Subset
IM
Grants
NIDDK NIH HHS · DK41816 · United States
NIDDK NIH HHS · DK53405 · United States
NHLBI NIH HHS · HL66225 · United States
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