正常人在餐後查血,也有可能出現“油質血(lipemia)”的狀況。但是如果空腹血脂很高,又有家族史,

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可以是家族性高血脂症,可以有不同種類型,而且多有其他臨床表現:

Familial hyperlipidemias

Fredrickson classification of hyperlipidemias
Hyperlipo-
proteinemia
OMIM Synonyms Defect Increased lipoprotein Main symptoms Treatment Serum appearance Estimated prevalence
Type I a 238600 Buerger-Gruetz syndrome or familial hyperchylomicronemia Decreased lipoprotein lipase (LPL) Chylomicrons Acute pancreatitis, lipemia retinalis, eruptive skin xanthomas, hepatosplenomegaly Diet control Creamy top layer One in 1,000,000[4]
b 207750 Familial apoprotein CII deficiency Altered ApoC2
c 118830   LPL inhibitor in blood
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 1 in 100
Type III 107741 Familial dysbetalipoproteinemia Defect in Apo E 2 synthesis IDL Tuboeruptive xanthomas and palmar xanthomas Fibrate, statins Turbid One in 10,000[5]
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
Type V 144650   Increased VLDL production and decreased LPL VLDL and chylomicrons   Niacin, fibrate Creamy top layer and turbid bottom  
 

Relative prevalence of familial forms of hyperlipoproteinemia[6]

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