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...

Полное описание

Библиографические подробности
Главные авторы: Franklin Hanna Rodriguez, Jorge Mario Estrada, Henry Mauricio Arenas Quintero, Juan Patricio Nogueira, Gloria Liliana Porras-Hurtado
Формат: Статья
Язык:English
Опубликовано: BMC 2023-03-01
Серии:Lipids in Health and Disease
Предметы:
Online-ссылка:https://doi.org/10.1186/s12944-022-01768-x