پديد آورندگان :
Noori، Noormohammad نويسنده Department of Pediatrics, Children and Adolescent Health Research Center, Zahedan University of Medical Sciences, Zahedan, Iran Noori, Noormohammad , Miri-Aliabad، Ghasem نويسنده Department of Pediatrics, Children and Adolescent Health Research Center, Zahedan University of Medical Sciences, Zahedan, Iran Miri-Aliabad, Ghasem , Jahantigh، Mehdi نويسنده Pathology Department, Faculty of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran ,
چكيده لاتين :
Familial hypercholesterolemia (FH) is an autosomal disorder that causes severe elevations in total cholesterol and low- density lipoprotein. FH is one of the primary risk factors for premature coronary artery disease in children and adults which requires early diagnosis and appropriate medical intervention. In this article, we report two cases of homozygous familial hypercholesterolemia.
