Cargando…
A novel lipoprotein lipase gene missense mutation in Chinese patients with severe hypertriglyceridemia and pancreatitis
BACKGROUND: Alterations or mutations in the lipoprotein lipase (LPL) gene contribute to severe hypertriglyceridemia (HTG). This study reported on two patients in a Chinese family with LPL gene mutations and severe HTG and acute pancreatitis. METHODS: Two patients with other five family members were...
Autores principales: | Chen, Tan-Zhou, Xie, Sai-Li, Jin, Rong, Huang, Zhi-Ming |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3983885/ https://www.ncbi.nlm.nih.gov/pubmed/24646025 http://dx.doi.org/10.1186/1476-511X-13-52 |
Ejemplares similares
-
Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants
por: Kassner, Ursula, et al.
Publicado: (2015) -
Management of severe hypertriglyceridemia due to lipoprotein lipase deficiency in children
por: Poon, Sarah W Y, et al.
Publicado: (2019) -
Severe Hypertriglyceridemia due to a novel p.Q240H mutation in the Lipoprotein Lipase gene
por: Soto, Angela Ganan, et al.
Publicado: (2015) -
A Novel Lipoprotein Lipase Mutation in an Infant With Glycogen Storage Disease Type-Ib and Severe Hypertriglyceridemia
por: Wang, Fengyu, et al.
Publicado: (2021) -
Lipoprotein Lipase: Is It a Magic Target for the Treatment of Hypertriglyceridemia
por: Moon, Joon Ho, et al.
Publicado: (2022)