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JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2005; 15 (9): 578-579
in English | IMEMR | ID: emr-71650

ABSTRACT

A case of familial hypercholesterolemia [homozygous] leading to coronary artery disease by the age of 10 years is presented in view of its rarity. Besides different xanthomatous eruptions, the child was also having overt angina and was treated with coronary artery bypass grafting to the diseased vessels


Subject(s)
Humans , Female , Hyperlipoproteinemia Type II/complications , Coronary Artery Disease/etiology , Homozygote , Xanthomatosis , Angina Pectoris , Coronary Artery Bypass , Lipoproteins, LDL
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