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Article

Familial Chylomicronemia Syndrome (FCS): Recent Data on Diagnosis and Treatment.

Current atherosclerosis reports - 27 Aug 2020

Gallo Antonio, Béliard Sophie, D'Erasmo Laura, Bruckert Eric

Abstract excerpt

PURPOSE OF REVIEW: Familial chylomicronemia syndrome (FCS) is a rare recessive genetic disorder often underdiagnosed with potentially severe clinical consequences. In this review, we describe the clinical and biological characteristics of the disease together with its main complication, i.e., acute pancreatitis. We focused the paper on new diagnostic tools, progress in understanding the role of two key proteins...

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Source

Identifiers

PMID: 32852651
DOI: 10.1007/s11883-020-00885-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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