Abstract
Background and Aims : Familial Hypercholesterolemia (FH) is an autosomal dominantly inherited disease commonly due to LDL Receptor Mutations. Heterozygous individuals are at risk of developing premature vascular disease due to accumulation of LDL. Early diagnosis and treatment are likely to reduce morbidity and mortality. To study the demographics, diagnostic features and response to therapy in adolescents with suspected FH .
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