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Accelerated Atherosclerosis in a Young Female with Familial Hypercholesterolemia
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作者 Adikesava Naidu Otikunta Praneeth Polamuri +3 位作者 Subba Reddy Y V Ravi Srinivas Ashok Thakkar arohi sarang 《International Journal of Clinical Medicine》 2014年第10期541-545,共5页
Familial hypercholesterolemia is an autosomal dominant genetic disease due to mutation in low-density lipoprotein-cholesterol receptor gene. It is characterized by elevated plasma low-density lipoprotein-cholesterol a... Familial hypercholesterolemia is an autosomal dominant genetic disease due to mutation in low-density lipoprotein-cholesterol receptor gene. It is characterized by elevated plasma low-density lipoprotein-cholesterol and the consequence of which leads to premature cardiovascular disease. The mainstay in the management of familial hypercholesterolemia patient is the treatment with high potency statin. However, current research shows influence of the type of low-density lipoprotein-cholesterol receptor mutations on severity of the cardiovascular disease, lipid profile, and response to statin treatment. We are here presenting a case of young Indian female patient who was diagnosed with familial hypercholesterolemia and treated with percutaneous transluminal coronary angioplasty in view of double vessel disease in the third decade of her life. She was prescribed with statin therapy for elevated low-density lipoprotein cholesterol. After 3 years, she presented once again with a triple vessel disease along with patent stented segments and abnormal lipid profile. 展开更多
关键词 FAMILIAL HYPERCHOLESTEROLEMIA PREMATURE CORONARY Artery Disease STATIN
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