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...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Society of Turaz Bilim
2022-03-01
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| Series: | Medicine Science |
| Subjects: | |
| Online Access: | http://www.ejmanager.com/fulltextpdf.php?mno=103899 |