can be a single gene disorder or multifactorial with complex inheritance patterns
primary
example of primary?
familial hypercholesteremia, an autosomal dominant receptor disease chromosome 19
elevated cholesterol in heterozygotes?
50% fewer receptors, 2-3x increase in total cholesterol
elevated cholesterol in homozygotes?
virtually no normal receptors, 5-6x increase in total cholesterol
clinical features of familial hypercholesteremia?
premature atherosclerosis
increased risk of MI
tendinous xanthomas
examples of secondary?
DM type I/II hypothyroidism renal failure alcohol ingestion liver disease
treatment?
statins (lovastatin)