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

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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Chi tiết về thư mục
Những tác giả chính: Franklin Hanna Rodriguez, Jorge Mario Estrada, Henry Mauricio Arenas Quintero, Juan Patricio Nogueira, Gloria Liliana Porras-Hurtado
Định dạng: Bài viết
Ngôn ngữ:English
Được phát hành: BMC 2023-03-01
Loạt:Lipids in Health and Disease
Những chủ đề:
Familial hyperchylomicronemia syndrome
Multifactorial chylomicronemia
Hypertriglyceridemia
Moulin FCS score
Truy cập trực tuyến:https://doi.org/10.1186/s12944-022-01768-x

Internet

https://doi.org/10.1186/s12944-022-01768-x

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