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Article

Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report.

Journal of medical case reports - 9 Jul 2020

Wickramasinghe Wasanthi, Karunathilaka Chathurika, Jayasinghe Saroj, Gooneratne Lallindra

Abstract excerpt

INTRODUCTION: Hereditary hemochromatosis is an inherited disorder of iron metabolism, characterized by excessive iron deposition in major organs of the body, leading to multi-organ dysfunction. It is a genetically heterogeneous disease caused by mutations in one or more different genes, the most common being mutations in the HFE gene. HFE hereditary hemochromatosis is mostly found in Europeans and is almost...

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Identifiers

PMID: 32641120
DOI: 10.1186/s13256-020-02428-3
PMCID: PMC7346448

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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