Type |
Synonym |
Defect |
Serum abnormality |
Clinical features |
Serum apperance |
Type - I |
Familial hyperchylomicrnemia |
Low LDL, Altered
Apo C- II |
Chylomicron |
Pancreatitis, Lipemia, retinalis,Skin eruptions, xanthoma, hepatosplenomegaly |
Creamy top layer |
Type - IIa |
Familial hypercholesterolemia |
LDL
receptor |
LDL |
Xanthelasma, Arcus senillis , Tendon xanthomas |
Clear |
Type- IIb |
Familial combined hypercholesterolemia |
LDL receptor &
Apo B |
LDL & VLDL |
|
Clear |
Type - III |
Familial dysbetalipoproteinemia |
Apo E2 synthesis defect |
IDL |
Tubo-eruptive xanthomas, palmar xanthoma |
Turbid |
Type – IV |
Familial hyperprebetalipoproteinemia |
VLDL production,
Elimination |
VLDL |
|
|
Type – V |
Endogenous hypertriglyceridemia |
VLDL
production,
LPL |
VLDL & Chylomicron |
|
Creamy top layer & turbid bottom. |