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What is Type I Hyperlipoproteinemia?
Familial hyperchylomicronemia
What is Type IIA Hyperlipoproteinemia?
Familial hypercholesterolemia
What is Type IIB Hyperlipoproteinemia?
Combined hyperlipidemia
What is Type III Hyperlipoproteinemia?
Familial dysbetalipoproteinemia
What is Type IV Hyperlipoproteinemia?
Familial hypertriglyceridemia
What is Type V Hyperlipoproteinemia?
Combined hypertriglyceridemia
LDL variant found in patients with obstructive jaundice and LCAT deficiency
LpX Lipoprotein
Same density as LDL and same size as VLDL but no Apo B
LpX Lipoprotein
Abnormal lipoprotein that accumulates in type 3 hyperlipoproteinemia and hepatic lipase deficiency
ẞ-VLDL Lipoprotein / Floating ẞ Lipoprotein
IDL with defective Apo E
ẞ-VLDL Lipoprotein / Floating ẞ Lipoprotein
Are abnormalities marked by decreased lipoprotein concentrations
HYPOLIPOPROTEINEMIA
– HDL concentrations as low as 1-2 mg/dL (0.03 – 0.05 mmol/L)
– Higher prevalence of CHD and stroke
Hypoalphalipoproteinemia
Defective Apo-A1
Familial Hypoalphalipoproteinemia
Defective ABCA1 transporter
Tangier Disease
Complete LCAT deficiency
Familial LCAT Deficiency
Partial LCAT deficiency
Fish Eye Disease
Low levels of LDL-cholesterol due to decreased production of Apo B-100
Hypobetalipoproteinemia
Decreased TAG export from liver = ?
FATTY LIVER DISEASE
Defect in microsomal triglyceride transfer protein (MTP)
Abetalipoproteinemia