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

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 of chylom...

Descripción completa

Detalles Bibliográficos
Autores principales: Rodriguez, Franklin Hanna, Estrada, Jorge Mario, Quintero, Henry Mauricio Arenas, Nogueira, Juan Patricio, Porras-Hurtado, Gloria Liliana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045250/
https://www.ncbi.nlm.nih.gov/pubmed/36978188
http://dx.doi.org/10.1186/s12944-022-01768-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045250/
https://www.ncbi.nlm.nih.gov/pubmed/36978188
http://dx.doi.org/10.1186/s12944-022-01768-x

Ejemplares similares