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Buy Wholesale and maintain an Active status for 2 months and we will refund your $39 Distributor Fee
07-SEPTEMBER-2008 03:17:44 - Dyslipidemia Redirected from Dyslipidaemia Dyslipidemia Classification and external resources ICD-10 E78. ICD-9 272 MeSH C18.452.339 Dyslipidemia is a disruption in the amount of lipids in the blood. In western societies, most dyslipidemias are hyperlipidemias; that is, an elevation of lipids in the blood, often due to diet and lifestyle. The prolonged elevation of insulin levels can lead to dyslipidemia. Increased levels of O-GlcNAc transferase OGT are known to cause dylipidaemia.1 Contents 1 Classification 2 Types 2.1 Increases 2.2 Decreases Classification There are two major ways in which dyslipidemias are classified: Phenotype, or the presentation in the body including the specific type of lipid that is increased Etiology, or the reason for the condition genetic, or secondary to another condition. This classification can be problematic, because most conditions involve the intersection of genetics and lifestyle issues. However, there are a few well defined genetic conditions that are usually easy to identify. Types Increases These conditions are discussed in greater detail at hyperlipidemia. Hyperlipidemia: lipids Hypercholesterolemia: cholesterol Hyperglyceridemia: glycerides Hypertriglyceridemia: triglycerides Hyperlipoproteinemia: lipoproteins usually LDL unless otherwise specified Hyperchylomicronemia: chylomicrons Combined hyperlipidemia: both LDL and triglycerides Familial hypercholesterolemia is a specific form of hypercholesterolemia due to a defect on chromosome 19 19p13.1-13.3. Decreases Hypolipoproteinemia: lipoproteins Hypocholesterolemia: cholesterol Abetalipoproteinemia: beta lipoproteins Tangier disease: high density lipoprotein This medical article is a stub. v d e Lipid metabolism disorders / Inborn error of lipid metabolism - dyslipidemia E78 and E71.3, 272 Hyperlipidemia Hypercholesterolemia/Hypertriglyceridemia Familial hypercholesterolemia, Combined hyperlipidemia - Xanthoma Hypolipoproteinemia Hypoalphalipoproteinemia/HDL Lecithin cholesterol acyltransferase deficiency, Tangier disease Hypobetalipoproteinemia/LDL Abetalipoproteinemia, Apolipoprotein B deficiency Lipodystrophy Barraquer-Simons syndrome Fatty acid metabolism deficiency transport: Carnitine Primary, I, II, -acylcarnitine - Adrenoleukodystrophy beta oxidation: Acyl CoA dehydrogenase Short-chain, Medium-chain, Long-chain 3-hydroxy, Very long-chain - Mitochondrial trifunctional protein deficiency to acetyl-CoA: Malonic aciduria Cholesterol synthesis Smith-Lemli-Opitz syndrome Other Sjögren-Larsson syndrome - Lipomatosis - Adiposis dolorosa - Lipoid proteinosis see also lipid metabolism enzymes, lipoprotein metabolism Retrieved from http://en..org/wiki/Dyslipidemia Categories: Medicine stubs | Metabolic disorders Views Article Discussion this page History Personal tools Log in / create account Navigation Main page Contents Featured content Current events Random article Search Go Search Interaction Community portal Recent changes Contact Donate to Help Toolbox What links here Related changes Upload file Special pages Printable version Permanent link Cite this page Languages Bahasa Indonesia Português Svenska Tiếng Việt 中文 This page was last modified on 12 June 2008, at 18:14
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So many of us do not eat a balanced diet, get enough sleep, have too much stress, or are impacted with toxins and pollutants. Drinking 2 ounces of MonaVie twice a day will help your body detoxify as well as build your immune system. Its the smartest thing you can do for yourself, so start today. Buying MonaVie through our company guarantees you support 7 days a week and, if you would like to share MonaVie with your family and friends we will guide you from start to finish.
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