Cargando…
A Comprehensive Update on the Chylomicronemia Syndrome
The chylomicronemia syndrome is characterized by severe hypertriglyceridemia and fasting chylomicronemia and predisposes affected individuals to acute pancreatitis. When due to very rare monogenic mutations in the genes encoding the enzyme, lipoprotein lipase, or its regulators, APOC2, APOA5, GPIHBP...
Autores principales: | Goldberg, Ronald B., Chait, Alan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644836/ https://www.ncbi.nlm.nih.gov/pubmed/33193106 http://dx.doi.org/10.3389/fendo.2020.593931 |
Ejemplares similares
-
Pregnancy in Familial Chylomicronemia Syndrome: Plasmapheresis as Therapeutic Approach
por: Leskovar, Dunja, et al.
Publicado: (2021) -
OR21-3 Familial Chylomicronemia Syndrome: Distinguishing the Rare Among the Common in Adults for Appropriate Management
por: Ueda, Masako, et al.
Publicado: (2019) -
Abdominal Pain as the Manifestation of Chylomicronemia Syndrome During Pregnancy: A Challenging Diagnosis
por: Parente, Catarina, et al.
Publicado: (2021) -
The Evolving Story of Multifactorial Chylomicronemia Syndrome
por: Paquette, Martine, et al.
Publicado: (2022) -
ODP153 Recurrent hypertriglyceridemia-induced pancreatitis due to multifactorial chylomicronemia syndrome in a patient with ketosis-prone diabetes mellitus
por: Thewjitcharoen, Yotsapon, et al.
Publicado: (2022)