What is another word for Mitochondrial Myopathies?
Pronunciation: [mˌa͡ɪtəkˈɒndɹɪəl ma͡ɪˈɒpəθɪz] (IPA) 
Mitochondrial myopathies are a group of rare genetic disorders that affect the mitochondria - the organelles that generate energy for the cells. These disorders are characterized by muscle weakness, fatigue, and pain, and may also cause vision and hearing problems, breathing difficulties, and gastrointestinal issues. Other terms that are commonly used to describe mitochondrial myopathies include mitochondrial disorders, mitochondrial encephalomyopathies, and mitochondrial diseases. Some specific types of mitochondrial myopathies have their own distinct names, such as Kearns-Sayre syndrome, MELAS syndrome, and Leigh syndrome. While there is no cure for mitochondrial myopathies, treatment may help to alleviate symptoms and improve quality of life.
