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...

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Detalhes bibliográficos
Publicado no:Case Rep Endocrinol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Hindawi 2020
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7149354/
https://ncbi.nlm.nih.gov/pubmed/32292609
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/1865489
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