Translations:Hyperlipidemia/9/en: Difference between revisions

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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
 |

|}