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14 Φεβ 2024 · We performed a retrospective chart review of adult patients diagnosed with mitochondrial myopathy at Mayo Clinic (2005–21). We identified 94 patients. Median time from symptom onset to diagnosis was 11 years (interquartile range 4–21 years).
- Understanding mitochondrial myopathies: a review - PMC
The goal of this review is to assess the current...
- Understanding mitochondrial myopathies: a review - PMC
Cardiopulmonary failure and acute cerebral events have been described as the leading cause of mortality in adult mitochondrial patients. 15 Patients with mitochondrial disease are more likely to have underlying myopathy, immobility, dysphagia, chronic intestinal pseudo-obstruction (CIPO), cardiomyopathy, and cardiac arrhythmias including Wolf ...
12 Ιουν 2024 · Specialists in the Mitochondrial Disease Clinic evaluate many types of mitochondrial diseases. Alpers progressive sclerosing poliodystrophy (Alpers disease). Barth syndrome.
The goal of this review is to assess the current understanding of mitochondrial diseases. This review focuses on the pathology, causes, risk factors, symptoms, prevalence data, symptomatic treatments, and new research aimed at possible preventions and/or treatments of mitochondrial diseases.
This review is aimed at a general medical and neurologist readership and provides a clinical approach to the recognition, investigation, and treatment of mitochondrial myopathies. Emphasis is placed on practical management considerations while including some recent updates in the field.
Features that can alert the clinician to mitochondrial myopathies include fatiguability, myalgia (often exercise-induced), exercise intolerance, and lactic acidaemia.
21 Μαΐ 2018 · Mitochondrial myopathies are mitochondrial diseases that cause prominent muscular symptoms such as muscle weakness and usually present with a multitude of symptoms and can affect virtually all organ systems. There is no cure for these diseases as of today. Treatment is generally supportive and emphasizes symptom management.
