SAT-565 Familial Homozygous Lipoprotein Lipase Defect Presenting with Recurrent Chylomicronemia Syndrome: Making a Case for Elective Plasmapheresis as an Adjuvant Treatment Modality

Background The chylomicronemia syndrome is a disorder characterized by severe hypertriglyceridemia and fasting chylomicronemia. Type Ia hyperlipoproteinemia is an extremely rare genetic disorder that results from homozygous deficiency in LPL activity. It is characterized by eruptive xanthomas, lipem...

Descripción completa

Detalles Bibliográficos
Autores principales: Shaka, Hafeez, Edigin, Ehizogie, Yap, Sara Elizabeth, Asemota, Iriagbonse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Cardiovascular Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208134/
http://dx.doi.org/10.1210/jendso/bvaa046.1507

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208134/
http://dx.doi.org/10.1210/jendso/bvaa046.1507

Ejemplares similares