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Message definition (Hyperlipidemia ) ! Defect ! Increased lipoprotein ! Main symptoms ! Treatment ! Serum appearance ! Estimated prevalence |- !rowspan=3| [[Type I hyperlipoproteinemia|Type I]] ! [[Hyperlipoproteinemia type Ia|a]] | {{OMIM|238600||none}} | Buerger-Gruetz syndrome or familial hyperchylomicronemia | Decreased [[lipoprotein lipase]] (LPL) |rowspan=3| [[Chylomicrons]] |rowspan=3| [[Acute pancreatitis]], [[lipemia retinalis]], eruptive skin [[xanthoma]]s, [[hepatosplenomegaly]] |rowspan=3| Diet control |rowspan=3| Creamy top layer |rowspan=3| One in 1,000,000 |- ! [[hyperlipoproteinemia type Ib|b]] | {{OMIM|207750||none}} | Familial apoprotein CII deficiency | Altered [[apolipoprotein C2|ApoC2]] |- ! [[Hyperlipoproteinemia type Ic|c]] | {{OMIM|118830||none}} | | [[Lipoprotein lipase|LPL]] inhibitor in blood |- !rowspan=2| Type II ! a | {{OMIM|143890||none}} | [[Familial hypercholesterolemia]] | [[LDL receptor]] deficiency | [[LDL]] | [[Xanthelasma]], [[arcus senilis]], tendon xanthomas | [[Bile acid sequestrant]]s, [[statin]]s, [[niacin (substance)|niacin]] | Clear | One in 500 for heterozygotes |- ! b | {{OMIM|144250||none}} | Familial combined hyperlipidemia | Decreased [[LDL receptor]] and increased [[apolipoprotein B|ApoB]] | [[LDL]] and [[VLDL]] | | Statins, niacin, [[fibrate]] | Turbid | One in 100 |- !colspan=2| Type III | {{OMIM|107741||none}} | [[Familial dysbetalipoproteinemia]] | Defect in [[apolipoprotein E|Apo E 2]] synthesis | [[Intermediate density lipoprotein|IDL]] | Tuberoeruptive xanthomas and palmar xanthomas | Fibrate, statins | Turbid | One in 10,000 |- !colspan=2| Type IV | {{OMIM|144600||none}} | [[Familial hypertriglyceridemia]] | Increased VLDL production and decreased elimination | VLDL |Can cause [[pancreatitis]] at high triglyceride levels | Fibrate, niacin, statins | Turbid | One in 100 |- !colspan=2| [[#type V|Type V]] | {{OMIM|144650||none}} | | Increased VLDL production and decreased [[Lipoprotein lipase|LPL]] | VLDL and chylomicrons | | Niacin, fibrate | Creamy top layer and turbid bottom | |}
! Defect
! Increased lipoprotein
! Main symptoms
! Treatment
! Serum appearance
! Estimated prevalence
|-
!rowspan=3| Type I
! a
| 238600
| Buerger-Gruetz syndrome or familial hyperchylomicronemia
| Decreased lipoprotein lipase (LPL)
|rowspan=3| Chylomicrons
|rowspan=3| Acute pancreatitis , lipemia retinalis , eruptive skin xanthomas , hepatosplenomegaly
|rowspan=3| Diet control
|rowspan=3| Creamy top layer
|rowspan=3| One in 1,000,000
|-
! b
| 207750
| Familial apoprotein CII deficiency
| Altered ApoC2
|-
! c
| 118830
|
| LPL inhibitor in blood
|-
!rowspan=2| Type II
! a
| 143890
| Familial hypercholesterolemia
| LDL receptor deficiency
| LDL
| Xanthelasma , arcus senilis , tendon xanthomas
| Bile acid sequestrants , statins , niacin
| Clear
| One in 500 for heterozygotes
|-
! b
| 144250
| Familial combined hyperlipidemia
| Decreased LDL receptor and increased ApoB
| LDL and VLDL
|
| Statins, niacin, fibrate
| Turbid
| One in 100
|-
!colspan=2| Type III
| 107741
| Familial dysbetalipoproteinemia
| Defect in Apo E 2 synthesis
| IDL
| Tuberoeruptive xanthomas and palmar xanthomas
| Fibrate, statins
| Turbid
| One in 10,000
|-
!colspan=2| Type IV
| 144600
| Familial hypertriglyceridemia
| Increased VLDL production and decreased elimination
| VLDL
|Can cause pancreatitis at high triglyceride levels
| Fibrate, niacin, statins
| Turbid
| One in 100
|-
!colspan=2| Type V
| 144650
|
| Increased VLDL production and decreased LPL
| VLDL and chylomicrons
|
| Niacin, fibrate
| Creamy top layer and turbid bottom
|
|}