Genetic screening for homozygous and heterozygous familial hypercholesterolemia

Familial hypercholesterolemia (FH) is a common inherited disorder that results in premature atherosclerosis. Diagnosis of FH is suspected on the basis of clinical criteria, but confirmation requires genetic testing. In the era of statins, early diagnosis and initiation of treatment can modify diseas...

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Detalles Bibliográficos
Autores principales: Izar, Maria C, Machado, Valéria A, Fonseca, Francisco A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681171/
https://www.ncbi.nlm.nih.gov/pubmed/23776359
http://dx.doi.org/10.2147/TACG.S13490

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681171/
https://www.ncbi.nlm.nih.gov/pubmed/23776359
http://dx.doi.org/10.2147/TACG.S13490

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