Patient with homozygous familial hypercholesterolemia: difficult to treat. Case report

Patient with homozygous familial hypercholesterolemia: difficult to treat. Case report

Homozygous familial hypercholesterolemia is a severe genetic disorder characterized by extremely high levels of total cholesterol and low-density lipoprotein cholesterol (LDL-C), as well as by rapid atherosclerosis progression in various vascular territories. Objective examination of the affected pa...

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Bibliographic Details
Main Authors: Andrey V. Susekov, Balakhonova T.V., Vladislav M. Soloviev, Yuliia S. Isaeva, Irina M. Miklashevich, Irina V. Leontieva
Format: Article
Language:English
Published: LLC "MEDIAFORMAT" 2020-01-01
Series:Клинический разбор в общей медицине
Subjects:
homozygous hypercholesterolemia
familial hypercholesterolemia
low-density lipoprotein cholesterol
rosuvastatin
ezetimibe
evolocumab
combination therapy
slowing the atherosclerosis progression
Online Access:https://klin-razbor.ru/en/archive/2020/vol-1-1-2020/patient-with-homozygous-familial-hypercholesterolemia-difficult-to-treat-case-report_5940/?element

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https://klin-razbor.ru/en/archive/2020/vol-1-1-2020/patient-with-homozygous-familial-hypercholesterolemia-difficult-to-treat-case-report_5940/?element

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