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Гомозиготна сімейна гіперхолестеринемія

ORPHA:391665· ICD-10 E78.0· Homozygous familial hypercholesterolemia

Визначення(English summary)

A rare disorder of lipid metabolism characterized by severely elevated plasma total cholesterol, low-density lipoprotein (LDL) cholesterol levels, and subsequent premature formation of atherosclerotic plaques in the coronary arteries, proximal aorta, and other arteries, significantly increasing the risk of premature cardiovascular disease and death. Xanthomas of the skin and in tendons are also a hallmark of the disease. Lethality is high due to early complications, in particular myocardial infarction and aortic valvular disease.

Поширеність
1-9 / 1 000 000
Успадкування
Autosomal dominant, Autosomal recessive
Вік початку
Neonatal