en هیپرکلسترولمی فامیلیال گزارش یک مورد گزارش مورد case report <p><strong>Abstract</strong></p> <p>Familial hypercholesterolemia (FH) is a hereditary dislipidemia. Patients present with extremely high level of low-density lipoprotein cholesterol (LDL-C), which is due to mutation in the gene of LDL receptor. Homozygous patients (HoFH) whose incidence is 1 in 1.000.000 are at high risk of premature aortic valve stenosis, and coronary artery atherosclerosis. In homozygous individuals cardiovascular complications can occur in childhood. The current study presented a 12-y-old boy with HoFH who suffered from mild aortic stenosis, and right coronary artery atherosclerosis. The patient underwent a successful coronary artery stenting, and was discharged with pharmacologic therapy.</p> Cardiovascular disease, Familial hypercholesterolemia, Homozygous form. 0 0 http://ijca.iums.ac.ir/browse.php?a_code=A-10-26-2&slc_lang=en&sid=1 Shahla Roodpeyma roodpeyma_shahla@yahoo.com 1003194753284600960 1003194753284600960 Yes Shahid beheshti University of Medical Sciences Sima Rafieyian sima_raf@yahoo.com 1003194753284600961 1003194753284600961 No the same as above Reza Shakeri rshakeri@yahoo.com 1003194753284600962 1003194753284600962 No same as above