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Article

Postprandial hypertriglyceridaemia in patients with Tangier disease.

Journal of clinical pathology - 1 Dec 2003

Kolovou G, Daskalova D, Anagnostopoulou K, Hoursalas I, Voudris V, Mikhailidis D P, Cokkinos D V

Abstract excerpt

BACKGROUND: Tangier disease (TD) is the phenotypic expression of rare familial syndromes with mutations in the ABCA1 transporter. TD results in extremely low high density lipoprotein (HDL) cholesterol and reduced low density lipoprotein cholesterol, with normal or mildly increased fasting triglyceride (TG) concentrations. Although there is a close relation between HDL cholesterol values and atherogenesis, the...

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Share to ABCA1 gene
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 14645354
DOI: 10.1136/jcp.56.12.937
PMCID: PMC1770132

Genes

ABCA1

Provenance

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.

Related research

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Postprandial hypertriglyceridaemia in patients with Tangier disease.PMID 14645354Read ↗

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Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency.Semantic proximity Read ↗

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Subfraction analysis of circulating lipoproteins in a patient with Tangier disease due to a novel ABCA1 mutation.Semantic proximity Read ↗

Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders.Semantic proximity Read ↗

Cellular cholesterol efflux in heterozygotes for Tangier disease is markedly reduced and correlates with high density lipoprotein cholesterol concentration and particle sizeSemantic proximity Read ↗

A novel ABCA1 mutation in Tangier disease associated with severe premature and rapidly progressive neurodegenerative disorder.Semantic proximity Read ↗

Tangier disease in family with the phenotype of familial hypercholesterolemia.Semantic proximity Read ↗

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The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease.Semantic proximity Read ↗

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