Homozygous familial hypercholesterolemia: modern aspects of pathogenesis, diagnostics and treatment

Homozygous familial hypercholesterolemia is a rare genetic disease featuring extremely high of low-density lipoprotein blood level, cutaneous and tendon xanthomas and accelerated atherosclerosis with often manifestions in the first 2 decades of life, resulting to premature death due to atheroscleros...

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Bibliografiska uppgifter
Huvudupphovsmän: V. К. Zafiraki, Е. D. Kosmacheva, I. N. Zakharova, V. A. Korneva, A. V. Susekov
Materialtyp: Artigo
Språk:Russo
Publicerad: Remedium Group LLC 2018-10-01
Serie:Медицинский совет
Ämnen:
homozygous familial hypercholesterolemia
atherosclerosis
lipid-lowering therapy
Länkar:https://www.med-sovet.pro/jour/article/view/2728
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