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| Mitochondrial myopathy Classification and external resources |
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| Simplified structure of a typical mitochondrion | |
| ICD-10 | G71.3 |
| MeSH | D017240 |
Mitochondrial myopathy are a type of myopathy associated with mitochondrial disease.
Treatment
Although no cure currently exists, there is some hope for a treatment for this whole class of hereditary diseases with the use of an embryotic mitochindrial transplant. [1]
Examples
Examples of Mitochondrial myopathy include:
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like syndrome (MELAS)
- varying degrees of cognitive impairment and dementia
- lactic acidosis
- strokes
- transient ischemic attacks
- hearing loss
- dysmotility
- weight loss
- Myoclonic epilepsy and ragged-red fibers (MERRF)
- progressive myoclonic epilepsy
- clumps of diseased mitochondria accumulate in the subsarcolemmal region of the muscle fiber and appear as "ragged-red fibers" when muscle is stained with modified Gomori trichrome stain
- short stature
- Kearns-Sayre syndrome (KSS)
- external ophthalmoplegia
- cardiac conduction defects
- sensory-neural hearing loss
- Progressive external ophthalmoplegia (PEO)
- progressive ophthalmoparesis is the cardinal feature
- symptomatic overlap with many other mitochondrial myopathies
References
- ^ "Three-parent embryo formed in lab" (web). Scientists believe they have made a potential breakthrough in the treatment of serious disease by creating a human embryo with three separate parents.. BBC News (Tuesday, 5 February 2008, 11:13 GMT). Retrieved on 2008-02-08.
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Wikipedia content modification information:
- This page was last modified on 6 May 2008, at 01:03.
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