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

Abstract Background 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 o...

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Principais autores:	Franklin Hanna Rodriguez, Jorge Mario Estrada, Henry Mauricio Arenas Quintero, Juan Patricio Nogueira, Gloria Liliana Porras-Hurtado
Formato:	Artigo
Idioma:	Inglês
Publicado:	BMC 2023-03-01
Series:	Lipids in Health and Disease
Assuntos:	Familial hyperchylomicronemia syndrome Multifactorial chylomicronemia Hypertriglyceridemia Moulin FCS score
Acceso en liña:	https://doi.org/10.1186/s12944-022-01768-x
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