Familial chylomicronemia syndrome: a case report

BACKGROUND: Familial chylomicronemia is an extremely rare disease. Lipoprotein lipase deficiency, lipoprotein defect or lipoprotein receptor defect are the main genetic causes of familial chylomicronemia. CASE PRESENTATION: We report a rare case of hypertriglyceridemia which was diagnosed at 24 days...

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Detalles Bibliográficos
Autores principales: Susheela, Ammu Thampi, Vadakapet, Padmesh, Pillai, Lekshmi, Thampi, Susheela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791813/
https://www.ncbi.nlm.nih.gov/pubmed/33419463
http://dx.doi.org/10.1186/s13256-020-02609-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791813/
https://www.ncbi.nlm.nih.gov/pubmed/33419463
http://dx.doi.org/10.1186/s13256-020-02609-0

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