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Article

Routine transferrin saturation measurement in liver clinic patients increases detection of hereditary haemochromatosis.

Annals of clinical biochemistry - 1 Sept 2003

Poullis A, Moodie S J, Ang L, Finlayson C J, Levin G E, Maxwell J D

Abstract excerpt

BACKGROUND: Hereditary haemochromatosis (HH) is one of the commonest genetic disorders in European populations. Transferrin saturation (TFS) measurement has been advocated as a phenotypic screening test to improve detection. We undertook a prospective study to examine the value of routine TFS measurement in detecting new cases of HH in unselected liver clinic attenders. METHODS: Non-fasting TFS was measured in...

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Identifiers

PMID: 14503989
DOI: 10.1258/000456303322326434

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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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