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  2. Hypolipoproteinemia - Wikipedia

    en.wikipedia.org/wiki/Hypolipoproteinemia

    Hypolipoproteinemia, hypolipidemia, or hypolipidaemia (British English) is a form of dyslipidemia that is defined by abnormally lowered levels of any or all lipids and/or lipoproteins in the blood. It occurs in genetic disorders (e.g. hypoalphalipoproteinemia , hypobetalipoproteinemia ), malnutrition , malabsorption , wasting disease , cancer ...

  3. Hypolipidemia - Wikipedia

    en.wikipedia.org/?title=Hypolipidemia&redirect=no

    Download as PDF; Printable version; ... move to sidebar hide. From Wikipedia, the free encyclopedia. Redirect page. Redirect to: Hypolipoproteinemia; Retrieved from ...

  4. Hypoalphalipoproteinemia - Wikipedia

    en.wikipedia.org/wiki/Hypoalphalipoproteinemia

    This genetic disorder article is a stub. You can help Wikipedia by expanding it.

  5. Dyslipidemia - Wikipedia

    en.wikipedia.org/wiki/Dyslipidemia

    Hypolipoproteinemia: lipoproteins. Abetalipoproteinemia: beta lipoproteins; Tangier disease: Tangier disease is an inherited disorder characterized by significantly reduced levels of high-density lipoprotein (HDL) in the blood. Both Combined hyperlipidemia: both LDL and triglycerides

  6. Hypobetalipoproteinemia - Wikipedia

    en.wikipedia.org/wiki/Hypobetalipoproteinemia

    Hypobetalipoproteinemia is a disorder consisting of low levels of LDL cholesterol or apolipoprotein B, [1] below the 5th percentile. [2] The patient can have hypobetalipoproteinemia and simultaneously have high levels of HDL cholesterol.

  7. Lecithin cholesterol acyltransferase deficiency - Wikipedia

    en.wikipedia.org/wiki/Lecithin_cholesterol_acyl...

    Lecithin cholesterol acyltransferase deficiency is a disorder of lipoprotein metabolism. [1] The disease has two forms: [2] Familial LCAT deficiency, in which there is complete LCAT deficiency, and Fish-eye disease, in which there is a partial deficiency.

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  9. Apolipoprotein B deficiency - Wikipedia

    en.wikipedia.org/wiki/Apolipoprotein_B_deficiency

    Apolipoprotein B deficiency is an autosomal dominant disorder resulting from a missense mutation which reduces the affinity of apoB-100 for the low-density lipoprotein receptor (LDL Receptor).