familial hyperlipoproteinemia type III

fa·mil·i·al hy·per·lip·o·pro·te·in·e·mi·a type III

[MIM*107741]
hyperlipoproteinemia characterized by increased plasma levels of LDL, β-lipoproteins, pre-β-lipoproteins, cholesterol, phospholipids, and triglycerides; hypertriglyceridemia induced by a high carbohydrate diet, and glucose tolerance is abnormal; frequent eruptive xanthomas and atheromatosis, particularly coronary artery disease; biochemical defect lies in apolipoproteins. There are many varieties, one of which is caused by mutation in the APOE gene on chromosome 19q.
Medical browser ?
Full browser ?