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These mutations generally affect tissues that have a high demand for metabolic energy production. Some disorders only affect a single organ, but many involve multiple organ systems

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13y ago
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1d ago

Mitochondrial myopathies typically affect tissues with high energy demands, such as skeletal muscles, heart muscles, and the central nervous system. Symptoms may include muscle weakness, exercise intolerance, and neurological problems due to impaired energy production.

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Q: What tissues are usually affected by mitochondrial myopathies?
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What are the characteristics of mitochondrial myopathies?

People affected with one of these disorders usually have muscle symptoms such as weakness, breathlessness, exercise intolerance, heart failure, dementia , stroke-like symptoms, deafness, blindness, seizures , heavy eyelids or eye problems, and/or vomiting


What are some congenital conditions classed as congenital myopathies?

Congenital myopathies are a group of myopathies, usually present from birth, that display structural changes in the skeletal muscles. The list of diseases defined as congenital myopathies varies.


When do the symptoms of mitochondrial myopathies caused by nDNA mutations usually develop?

Generally, nDNA mutations result in clinical symptoms that develop during early childhood, while mtDNA mutations (either directly or as secondary effects from a nDNA mutation) lead to clinical manifestations that develop in late childhood


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Progressive myopathies that develop later in life usually have a better prognosis than conditions that develop during childhood.


How would you describe the medical condition myopathy?

Skeletal muscle diseases, or myopathies, are disorders with structural changes or functional impairment of the muscle, usually presenting as muscle weakness.


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