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Article

Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage disease.

QJM : monthly journal of the Association of Physicians - 1 Sept 1998

Kelly A L, Rhodes D A, Roland J M, Schofield P, Cox T M

Abstract excerpt

Juvenile haemochromatosis is a rare inborn error of iron metabolism with clinical manifestations before 30 years of age. Unlike adult haemochromatosis which principally affects men, juvenile haemochromatosis affects the sexes equally; it causes early endocrine failure, dilated cardiomyopathy and joint disease. We report four patients (two of each sex) from three pedigrees affected by juvenile haemochromatosis...

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Source

Identifiers

PMID: 10024915
DOI: 10.1093/qjmed/91.9.607

Genes

HFE

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage disease.PMID 10024915Read ↗

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