The burden of familial chylomicronemia syndrome in Canadian patients

BACKGROUND: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder characterized by persistent extreme hypertriglyceridemia as a result of lipoprotein lipase deficiency. Canada is an important region for FCS research due to the high prevalence rates. The burden of illness and...

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Detalles Bibliográficos
Autores principales: Gaudet, Daniel, Stevenson, Michael, Komari, Nelly, Trentin, Grace, Crowson, Caroline, Hadker, Nandini, Bernard, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268343/
https://www.ncbi.nlm.nih.gov/pubmed/32487261
http://dx.doi.org/10.1186/s12944-020-01302-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268343/
https://www.ncbi.nlm.nih.gov/pubmed/32487261
http://dx.doi.org/10.1186/s12944-020-01302-x

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