Homozygous Familial Hypercholesterolemia (HoFH) in Saudi Arabia and Two Cases of Lomitapide Use in a Real-World Setting

INTRODUCTION: Homozygous familial hypercholesterolemia (HoFH) is a rare, genetic condition in which mutations in key peptides involved in the low-density lipoprotein receptor (LDL-R) pathway result in markedly elevated levels of circulating LDL-cholesterol (LDL-C). Patients are at high risk of devel...

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Detalles Bibliográficos
Autores principales: Mahzari, Moeber, Zarif, Hawazen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107066/
https://www.ncbi.nlm.nih.gov/pubmed/33829367
http://dx.doi.org/10.1007/s12325-021-01720-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107066/
https://www.ncbi.nlm.nih.gov/pubmed/33829367
http://dx.doi.org/10.1007/s12325-021-01720-y

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