Challenges in familial chylomicronemia syndrome diagnosis and management across latin american countries: an expert panel discussion
Familial chylomicronemia syndrome (FCS) is a rare genetic disorder characterized by extremely high triglyceride levels due to impaired clearance of chylomicrons from plasma. This paper is the result of a panel discussion with Latin American specialists who raised the main issues on diagnosis and man...
- Autores:
-
Lorenzatti, Alberto J.
Nogueira, Juan Patricio
Cafferata, Alberto M.
Aimone, Daniel
Lourenco, Charles Marques
Izar, Maria Cristina De Oliveira
de Lima, Josivan Gomes
Lottenberg Pita, Ana Maria
Alonso, Rodrigo
Garay, Karla
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2021
- Institución:
- Universidad El Bosque
- Repositorio:
- Repositorio U. El Bosque
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.unbosque.edu.co:20.500.12495/7066
- Palabra clave:
- FCS
Familial chylomicronemia syndrome
Hypertriglyceridemia
Clinical phenotype
- Rights
- openAccess
- License
- Acceso abierto