Challenges in the Diagnosis and Treatment of Homozygous Familial Hypercholesterolemia

Homozygous familial hypercholesterolemia (HoFH) is a rare, genetic disorder characterized by an absence or impairment of low-density lipoprotein receptor (LDLR) function resulting in significantly elevated low-density lipoprotein cholesterol (LDL-C) levels. The cholesterol exposure burden beginning...

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Detalles Bibliográficos
Autores principales: Ito, Matthew K., Watts, Gerald F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Therapy in Practice
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611011/
https://www.ncbi.nlm.nih.gov/pubmed/26370207
http://dx.doi.org/10.1007/s40265-015-0466-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611011/
https://www.ncbi.nlm.nih.gov/pubmed/26370207
http://dx.doi.org/10.1007/s40265-015-0466-y

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