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Article

A 60-y-old chylomicronemia patient homozygous for missense mutation (G188E) in the lipoprotein lipase gene showed no accelerated atherosclerosis.

Clinica chimica acta; international journal of clinical chemistry - 1 Jan 2000

Ebara Tetsu, Endo Yoriko, Yoshiike Shouichi, Tsuji Masatomi, Taguchi Susumu, Murase Toshio, Okubo Minoru

Abstract excerpt

BACKGROUND: Familial lipoprotein lipase (LPL) deficiency is a rare autosomal recessive disorder caused by mutations in the LPL gene. Patients with LPL deficiency have chylomicronemia; however, whether they develop accelerated atherosclerosis remains unclear. METHODS: We investigated clinical and mutational characteristics of a 60-y-old Japanese patient with chylomicronemia. RESULTS: The patient's fasting plasma...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperlipoproteinemia Type I

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Share to Tomography, X-Ray Computed

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Source

Identifiers

PMID: 17854791
DOI: 10.1016/j.cca.2007.08.011

Genes

LPL

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.

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A 60-y-old chylomicronemia patient homozygous for missense mutation (G188E) in the lipoprotein lipase gene showed no accelerated atherosclerosis.PMID 17854791Read ↗

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