Mitochondrial myopathies are a group of diseases that affect the mitochondria. These are tiny structures found in almost all cells. It is their job to provide energy to these cells. These diseases can make it hard for the body to function as it should. The muscles and nerves are most affected.
Mitochondrial myopathies decrease the ability of nerves and muscles. Weakness and uncoordinated movement may result.
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This health problem is caused by a mutation in a specific gene.
The risk of this problem is higher in people who have a family member with the mutated gene.
Muscle fatigue, pain, and weakness are the main symptoms. Other symptoms depend on which cells of the body are affected. Problems can be mild to severe and they vary from person to person.
Some common problems may be:
|NAME OF DISEASE||WHEN IT STARTS||SYMPTOMS|
|Kearns-Sayre syndrome (KSS)||Before age 20||Salt and pepper eye color, eye movement problems, and heart and skeletal muscle problems|
|Barth syndrome||Infancy||Heart muscle problems and frequent infections|
|Leigh’s syndrome||Infancy—can appear later||Changes with how the brain works, seizures, poor vision and hearing, developmental delay, and problems breathing|
|Mitochondrial DNA depletion syndrome||Infancy||Liver failure, muscle floppiness, feeding problems, and developmental delay|
|Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)||Childhood to adulthood||Stroke-like episodes, migraine headaches, vomiting and seizures, muscle weakness, exercise intolerance, hearing loss, diabetes, and short stature|
|Myoclonic epilepsy associated with ragged red fibers (MERRF)||Late childhood to adulthood||Jerky muscle movements, seizures, muscle weakness, and uncoordinated muscle movements|
|Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)||Before age 20||Eye movement problems, drooping eyelid, limb weakness, and digestive problems|
|Neuropathy, ataxia, and retinitis pigmentosa (NARP)||Early childhood to adulthood||Uncoordinated muscle movement and vision problems|
|Pearson’s syndrome||Infancy||Anemia, problems with the pancreas, development of KSS|
|Progressive external ophthalmoplegia (PEO)||Adolescence or adulthood||Eye movement problems, and often symptoms of other mitochondrial diseases, but can be an independent syndrome|
The doctor will ask about your symptoms and health history. You will also be asked about any family history of the disease. A physical exam will be done. An eye exam may also be done.
Your body fluids and tissues may be tested. This can be done with:
The heart's electrical activity may be tested. This can be done with an electrocardiogram (EKG).
Nerve function may be tested. This can be done with electromyography (EMG).
There is no cure. The goal is to manage symptoms. Options are:
Supplements may help the cells make energy. These may be:
Therapy may be:
Medicines may be needed to manage specific symptoms, such as irregular heartbeat, seizures, or pain.
There are no current guidelines to prevent this health problem.
Muscular Dystrophy Association
National Institute of Neurological Disorders and Stroke
Canadian Institutes of Health Research
Muscle Dystrophy Canada
Mitochondrial myopathies (MM). Muscular Dystrophy Association website. Available at: https://www.mda.org/disease/mitochondrial-myopathies. Accessed August 19, 2021.
Mitochondrial myopathies information page. National Institute of Neurological Disorders and Stroke website. Available at: https://www.ninds.nih.gov/Disorders/All-Disorders/Mitochondrial-Myopathy-Information-Page. Accessed August 19, 2021.
Mitochondrial myopathy. National Organization of Rare Disorders website. Available at: https://rarediseases.org/physician-guide/mitochondrial-myopathy. Accessed August 19, 2021.
Overview of metabolic myopathies. EBSCO DynaMed website. Available at: https://www.dynamed.com/condition/overview-of-metabolic-myopathies. Accessed August 19, 2021.
Last reviewed July 2021 by EBSCO Medical Review Board James Cornell, MD Last Updated: 8/19/2021