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A very rare disease. It causes developmental issues or muscle weakness.

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It is a mutation or change in the genes. It can be only be inherited by the mother. you cannot catch it you are born with it.

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It depends what parts of the body is affected by the disease. Some might live a normal life with few issues but for some people they can have more intense symptoms.
Some symptoms can be
- hearing loss
- kidney failure
- strokes
- seizures
- heart failure
and more...

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 ❮What can someone do with this disease?❯

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 ❮What can someone do with this disease?❯

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There is no cure for this. There is treatment to help with symptoms. The treatment options is different for each person. Some ways people treat this is just by having a diet and exercise or taking Dietary Supplements.

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yes it can. they use it to see if a person does have this rare disorder.

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Works Cited

“Diseases - MM - Causes/Inheritance.” Muscular Dystrophy Association, 18 Dec. 2015, www.mda.org/disease/mitochondrial-myopathies/causes-inheritance#:~:text=Mitochondrial%20diseases%20are%20not%20contagious.

“Mitochondrial Disease | Symptoms & Causes | Boston Children’s Hospital.” Www.childrenshospital.org, www.childrenshospital.org/conditions-and-treatments/conditions/m/mitochondrial-disease/symptoms-and-causes#:~:text=The%20parts%20of%20the%20body. Accessed 20 May 2021.

“Mitochondrial Disease: Read about Treatment and Symptoms.” MedicineNet, www.medicinenet.com/mitochondrial_disease/article.htm#mitochondrial_myopathies_facts. Accessed 20 May 2021.

“Mitochondrial Diseases: Causes, Symptoms, Diagnosis & Treatment.” Cleveland Clinic, my.clevelandclinic.org/health/diseases/15612-mitochondrial-diseases#:~:text=There%20are%20no%20cures%20for. Accessed 20 May 2021.

Nesbitt, Victoria, et al. “A National Perspective on Prenatal Testing for Mitochondrial Disease.” European Journal of Human Genetics, vol. 22, no. 11, 19 Mar. 2014, pp. 1255–1259, 10.1038/ejhg.2014.35. Accessed 29 Mar. 2021.