Phenotypic vs. genetic cascade screening for familial hypercholesterolemia: A case report

One of the most common autosomal dominant disorders is familial hypercholesterolemia (FH), causing premature atherosclerotic cardiovascular diseases and a high risk of death due to lifelong exposure to elevated low-density lipoprotein cholesterol (LDL-C) levels. FH has a proven arsenal of treatments...

Descripció completa

Dades bibliogràfiques

Autors principals:	Anastasia V. Blokhina, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Marina V. Klimushina, Anastasia A. Zharikova, Evgeniia A. Sotnikova, Vasily E. Ramensky, Oxana M. Drapkina
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2022-08-01
Col·lecció:	Frontiers in Cardiovascular Medicine
Matèries:	familial hypercholesterolemia cascade screening phenotypic screening genetic screening molecular genetic testing LDLR
Accés en línia:	https://www.frontiersin.org/articles/10.3389/fcvm.2022.982607/full
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!