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Myopathy
(redirected from myopathic)

   Also found in: Dictionary/thesaurus, Medical, Wikipedia 0.03 sec.
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.

REFERENCES

Badalian, 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



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Research in genetic mitochondrial diseases shows not simply myopathic changes, but also marked hypothalamic disruption.
JS, a 58-year-old man, was diagnosed with an inflammatory myopathy on the basis of: proximal weakness, elevated creatinine kinase (CK) (7 000) and a myopathic picture on electromyography.
Intramuscular ubiquinone levels do not decrease, however, making ubiquinone an unlikely cause of the myopathy (8), although only one study no studies to our knowledge have examined ubiquinone levels in statin myopathic patients (9).
 
 
 
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