Article

Analyses of Familial Chylomicronemia Syndrome And Multifactorial Chylomicronemia In Colombia 2010-2020: A Cross-Sectional Study

2022-10-21

Abstract excerpt

<h4>Background: </h4> and aim Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive metabolic disorder caused by mutations in genes involved in chylomicron metabolism. On the other hand, multifactorial chylomicronemia syndrome (MCS) is a polygenic disorder and the most frequent cause of chylomicronemia, which results from the presence of multiple genetic variants related to chylomicron metabolism,...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: abd9c6a8-dfd4-5f0a-8182-b0f99d092f03
DOI: 10.21203/rs.3.rs-2154973/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Analyses of Familial Chylomicronemia Syndrome And Multifactorial Chylomicronemia In Colombia 2010-2020: A Cross-Sectional StudyDOI 10.21203/rs.3.rs-2154973/v1Read

Analyses of familial chylomicronemia syndrome in Pereira, Colombia 2010–2020: a cross-sectional studySemantic proximity Read

Multifactorial chylomicronemia: keys to detecting severe forms.Semantic proximity Read

Clinical identification of familial chylomicronemia syndrome and novel therapeutic options.Semantic proximity Read

A novel homozygous variant in GPIHBP1: A case series of familial chylomicronemia syndrome from Colombia.Semantic proximity Read

Spectrum of Mutations and Long-Term Clinical Outcomes in Genetic Chylomicronemia SyndromesSemantic proximity Read

Comprehensive analysis of Chinese patients with non-LPL familial chylomicronemia syndrome: Genetic variants, dietary interventions, and clinical insights.Semantic proximity Read

Causes, clinical findings and therapeutic options in chylomicronemia syndrome, a special form of hypertriglyceridemia.Semantic proximity Read

Application of the North American Familial Chylomicronemia Syndrome Score (NAFCS Score) in monogenic hypertriglyceridemia patients: A single-center Turkish cohort study.Semantic proximity Read

Genome Sequencing Identifies Monogenic Causes in Adults with Metabolic DiseasesSemantic proximity Read

Contemporary Management of Familial and Multifactorial Chylomicronemia Syndromes in Italy: Insights From the National LIPIGEN Registry.Semantic proximity Read

Genetics of Hypertriglyceridemia.Semantic proximity Read

Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an "FCS score".Semantic proximity Read