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  2. Fatty-acid metabolism disorder - Wikipedia

    en.wikipedia.org/wiki/Fatty-acid_metabolism_disorder

    Individuals with a fatty-acid metabolism disorder are unable to metabolize this fat source for energy, halting bodily processes. [1] Most individuals with a fatty-acid metabolism disorder are able to live a normal active life with simple adjustments to diet and medications. If left undiagnosed many complications can arise.

  3. Very long-chain acyl-coenzyme A dehydrogenase deficiency

    en.wikipedia.org/wiki/Very_long-chain_acyl...

    Very long-chain acyl-coenzyme A dehydrogenase deficiency is a fatty-acid metabolism disorder which prevents the body from converting certain fats to energy, particularly during periods without food. [1] [2] [3] Those affected by this disorder have inadequate levels of an enzyme that breaks down a group of fats called very long-chain fatty acids.

  4. Anti-obesity medication - Wikipedia

    en.wikipedia.org/wiki/Anti-obesity_medication

    Bimagrumab, an experimental drug, works by inhibiting the action of myostatin, which limits the size of skeletal muscle. The drug has shown the ability to increase lean mass simultaneously to decreasing fat mass in obese humans, which is beneficial because it preserves or increases energy expenditure while reducing risks associated with excess fat.

  5. How to preserve muscle mass on weight-loss drugs like Wegovy

    www.aol.com/preserve-muscle-mass-weight-loss...

    There is some debate as to whether GLP-1 agonist drugs like Wegovy can lead to unhealthy muscle mass loss in addition to general weight loss. ... the muscle tissue shows an accumulation of fat and ...

  6. Is Ozempic the New Anti-Inflammatory Wonder Drug? - AOL

    www.aol.com/ozempic-anti-inflammatory-wonder...

    Finally, I started her on a relatively new injectable drug called Gattex (teduglutide), an analogue of a human hormone secreted by intestinal cells known as glucagon-like peptide-2 (GLP-2).

  7. Lipid storage disorder - Wikipedia

    en.wikipedia.org/wiki/Lipid_storage_disorder

    Many lipid storage disorders can be classified into the subgroup of sphingolipidoses, as they relate to sphingolipid metabolism. Members of this group include Niemann-Pick disease, Fabry disease, Krabbe disease, Gaucher disease, Tay–Sachs disease, metachromatic leukodystrophy, multiple sulfatase deficiency, and Farber disease.

  8. Chylomicron retention disease - Wikipedia

    en.wikipedia.org/wiki/Chylomicron_retention_disease

    The symptoms of CmRD are similar to the physical symptoms of malnutrition, as the disease arises due to the poor absorption of lipids and fat-soluble nutrients such as vitamin E. For this reason, the disease is likely to be underdiagnosed by physicians. Fat-soluble nutrients are essential for growth, development, and normal bodily function.

  9. Familial multiple lipomatosis - Wikipedia

    en.wikipedia.org/wiki/Familial_Multiple_Lipomatosis

    Hormonal disorder due to the body's inability to properly metabolize fat; Increase in fat cells ; Enzymatic defect or a change in the surface of the cells that could prevent the breakdown of fat; Poor lymphatic drainage; Defective regulation of mitochondria in brown fat. Brown fat is responsible for causing heat in times of stress or cold.