Familial Hypercholesterolemia and Its Current Diagnostics and Treatment Possibilities: A Literature Analysis

Familial hypercholesterolemia (FH) is a common, inherited disorder of cholesterol metabolism. This pathology is usually an autosomal dominant disorder and is caused by inherited mutations in the APOB, LDLR, and PCSK9 genes. Patients can have a homozygous or a heterozygous genotype, which determines...

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Detalles Bibliográficos
Autores principales: Zubielienė, Kristina, Valterytė, Gintarė, Jonaitienė, Neda, Žaliaduonytė, Diana, Zabiela, Vytautas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692978/
https://www.ncbi.nlm.nih.gov/pubmed/36422206
http://dx.doi.org/10.3390/medicina58111665

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692978/
https://www.ncbi.nlm.nih.gov/pubmed/36422206
http://dx.doi.org/10.3390/medicina58111665

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