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...

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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
Acceso en línea:
http://hdl.handle.net/20.500.12495/7066
https://doi.org/10.1016/j.jacl.2021.10.004
Palabra clave:
FCS
Familial chylomicronemia syndrome
Hypertriglyceridemia
Clinical phenotype
Rights
openAccess
License
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