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Myopathy |
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myopathy [mī′äp·ə·thē]
(medicine) Any disease of the muscles. Also known as myopathia. Myopathy progressive muscular dystrophy; a hereditary disease. Myopathies can be transmitted as autosomal recessive or dominant, or sex chromosome-linked traits. Myopathies result from metabolic disturbances in muscle cells and a change in the biosynthesis of nucleic acids; the degradation of muscle proteins is considerably more rapid than their biosynthesis. In myopathies, muscles become flaccid and some of the fibers are replaced by fatty tissue. Electron microscopy reveals structural changes in the membranes of muscle cells. The main symptoms of the disease are increasing muscular weakness, symmetrical muscular atrophy, decrease in tendon reflexes and, in the later stages, bone and joint deformity. Autonomic trophic nerve functions are invariably impaired. Myopathy is treated with anticholinesterase preparations, anabolic hormones, and vitamins B and E. Preventive measures include early diagnosis and detection of the heterozygous carrier state for the myopathy gene by using electrophysiological and biochemical tests. REFERENCESBadalian, L. O., V. A. Tabolin, and Iu. V. Vel’tishchev. Nasledstvennye bolezni u detei. Moscow, 1971.Hausmanowa-Petrusewicz, I. Myshechnye zabolevaniia. Warsaw, 1971. (Translated from Polish.) L. O. BADALIAN Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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No references found | Contributions cover acute neuropathies, chronic inflammatory demyelinating neuropathy and its variants, nonsystemic vasculitic neuropathy, dysimmune neuropathy, autoimmune autonomic ganglionopathy, myasthenia gravis with anti-acetylcholine receptor antibodies, muscle-specific receptor tyrosine kinase antibody-positive and seronegative myasthenia gravis, Lambert-Eaton myasthenic syndrome, idiopathic inflammatory myopathies, and stiff person syndrome. They include muscle-wasting mitochondrial myopathies, Leber's Hereditary Optic Neuropathy which leads to blindness, nerve illnesses similar to multiple sclerosis, and conditions that damage organs, including the heart. In future, the same technique could be used to rid human embryos of bad mitochondria, and the disorders they cause, which include muscle-wasting mitochondrial myopathies, Leber's Hereditary Optic Neuropathy which leads to blindness, and nerve illnesses similar to multiple sclerosis. |
myopathies |
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