enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. 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

  4. Hypoalphalipoproteinemia - Wikipedia

    en.wikipedia.org/wiki/Hypoalphalipoproteinemia

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

  5. Lipoprotein lipase deficiency - Wikipedia

    en.wikipedia.org/wiki/Lipoprotein_lipase_deficiency

    The diagnosis of familial lipoprotein lipase deficiency is finally confirmed by detection of either homozygous or compound heterozygous pathogenic gene variants in LPL with either low or absent lipoprotein lipase enzyme activity. [citation needed] Lipid measurements · Milky, lipemic plasma revealing severe hyperchylomicronemia; [citation needed]

  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. Tangier disease - Wikipedia

    en.wikipedia.org/wiki/Tangier_disease

    After initial diagnosis with Niemann-Pick he was transferred to Dr. Louis Avioli at the National Cancer Institute. Donald Fredrickson, then head of the Molecular Disease Branch, became aware of the case and had a hunch that the original diagnosis was incorrect. In 1960, he traveled with Dr. Avioli to Tangier Island for further investigation.

  8. 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.

  9. Abetalipoproteinemia - Wikipedia

    en.wikipedia.org/wiki/Abetalipoproteinemia

    Despite the relatively late diagnosis, the patient married and at the age of 34, gave birth to a full-term healthy infant. Her medication included vitamin K 10 mg twice a week, beta-carotene 40,000 IU daily, vitamin A 10,000 IU daily, vitamin E 400 IU daily, vitamins B6 and B12, calcium, magnesium and eye drops.