Familial dysbetalipoproteinemia or type III hyperlipoproteinemia is a condition characterized by increased total cholesterol and triglyceride levels,...
4 KB (290 words) - 20:13, 30 October 2024
Hyperlipidemia (redirect from Familial apoprotein CII deficiency)
(intermediate density lipoprotein). Also known as broad beta disease or dysbetalipoproteinemia, the most common cause for this form is the presence of ApoE E2/E2...
46 KB (4,438 words) - 19:51, 14 November 2024
Abetalipoproteinemia (redirect from Familial hypobetalipoproteinemia)
chylomicrons and VLDL respectively. It is not to be confused with familial dysbetalipoproteinemia. It is a rare autosomal recessive disorder. Initial symptoms...
21 KB (2,253 words) - 12:35, 20 October 2024
clusters on the skin of the trunk, buttocks and extremities. Familial dysbetalipoproteinemia causes larger, tuberous xanthomas; these are red or orange...
17 KB (1,614 words) - 22:05, 22 November 2024
metabolism and cardiovascular disease. Defects in APOE result in familial dysbetalipoproteinemia aka type III hyperlipoproteinemia (HLP III), in which increased...
57 KB (6,407 words) - 08:57, 18 October 2024
hyperlipoproteinemia) Familial defective apolipoprotein B-100 Familial dysbetalipoproteinemia (broad beta disease, remnant removal disease) Familial hypertriglyceridemia...
198 KB (17,956 words) - 10:27, 2 November 2024
Havekes LM, Frants RR (May 1988). "Exact localization of the familial dysbetalipoproteinemia associated HpaI restriction site in the promoter region of...
13 KB (1,552 words) - 18:05, 24 January 2024
hypercholesterolemia Hypertriglyceridemia (Fredrickson Type IV) Primary dysbetalipoproteinemia (Fredrickson Type III) Combined hyperlipidemia Primary prevention...
100 KB (9,454 words) - 15:22, 12 November 2024