Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon

Familial chylomicronemia syndrome is a rare autosomal recessive disorder of lipoprotein metabolism characterized by the presence of chylomicrons in fasting plasma and an important increase in plasma triglycerides (TG) levels that can exceed 22.58 mmol/l. The disease is associated with recurrent epis...

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Detalles Bibliográficos
Autores principales: Ayoub, Carine, Azar, Yara, Maddah, Dina, Ghaleb, Youmna, Elbitar, Sandy, Abou-Khalil, Yara, Jambart, Selim, Varret, Mathilde, Boileau, Catherine, El Khoury, Petra, Abifadel, Marianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437297/
https://www.ncbi.nlm.nih.gov/pubmed/36061186
http://dx.doi.org/10.3389/fgene.2022.961028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437297/
https://www.ncbi.nlm.nih.gov/pubmed/36061186
http://dx.doi.org/10.3389/fgene.2022.961028

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