Treatment and follow-up of coronary artery disease in a child with homozygous familial hypercholesterolemia

Treatment and follow-up of coronary artery disease in a child with homozygous familial hypercholesterolemia

Familial hypercholesterolemia is a metabolic disease caused by a mutation in the low-density lipoprotein receptor gene. It carries early atherosclerosis and coronary artery disease risks. Coronary artery disease has been reported 20 times in the pediatric population with familial hypercholesterolemi...

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Bibliographic Details
Main Authors: Mehmet Oncul, Cemsit Karakurt, Ozlem Elkiran, Aysehan Akinci, Nevzat Erdil
Format: Article
Language:English
Published: Society of Turaz Bilim 2022-03-01
Series:Medicine Science
Subjects:
familial hypercholesterolemia
atherosclerosis
cardiovascular disease
coronary artery stenosis
children
Online Access:http://www.ejmanager.com/fulltextpdf.php?mno=103899

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