Saturday, October 31, 2020
Mitochondrial Health

Primary mitochondrial myopathy – causes, symptoms, diagnosis, treatment, pathology



What is Primary mitochondrial myopathy? Primary mitochondrial myopathy is a rare genetic disorder that occurs when there are mutated mitochondria in muscle cells, especially skeletal muscle cells.

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10 thoughts on “Primary mitochondrial myopathy – causes, symptoms, diagnosis, treatment, pathology
  1. Thank you so much for making such an informative and interesting medical videos I have been watching these videos since 1 year
    Just a single request that pls make videos little longer and little more elaborative so we can understand better
    Thank you 😊

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