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Article

The familial chylomicronemia syndrome.

Endocrinology and metabolism clinics of North America - 1 Sept 1998

Santamarina-Fojo S

Abstract excerpt

The chylomicronemia syndrome is a disorder characterized by severe hypertriglyceridemia and fasting chylomicronemia. Genetic causes of the syndrome are rare and include deficiency of lipoprotein lipase (LPL), apolipoprotein C-II, and familial inhibitor of LPL. Patients with familial forms of hypertriglyceridemia in combination with secondary acquired disorders account for most individuals presenting with...

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Source

Identifiers

PMID: 9785052
DOI: 10.1016/s0889-8529(05)70025-6

Genes

LPL

Provenance

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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