Experimental Therapeutics for Challenging Clinical Care of a Patient with an Extremely Rare Homozygous APOC2 Mutation

BACKGROUND: Among many causes of hypertriglyceridemia (HTG), familial chylomicronemia syndrome (FCS) is a rare monogenic disorder that manifests as severe HTG and acute pancreatitis. Among the known causal genes for FCS, mutations in APOC2 only account for <2% of cases. Medical nutrition therapy...

Descripción completa

Detalles Bibliográficos
Autores principales: Ueda, Masako, Wolska, Anna, Burke, Frances M., Escobar, Maria, Walters, Laura, Lalic, Dusanka, Hegele, Robert A., Remaley, Alan T., Rader, Daniel J., Dunbar, Richard L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149354/
https://www.ncbi.nlm.nih.gov/pubmed/32292609
http://dx.doi.org/10.1155/2020/1865489

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149354/
https://www.ncbi.nlm.nih.gov/pubmed/32292609
http://dx.doi.org/10.1155/2020/1865489

Ejemplares similares