Mitochondrial myopathies

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Mitochondrial myopathy
Classification and external resources
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:

  • 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

References

  1. ^ "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.

Wikipedia content modification information:

  • This page was last modified on 6 May 2008, at 01:03.

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