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Metabolic myopathies are myopathies that result from defects in biochemical metabolism that primarily affect muscle. They are generally genetic defects that interfere with muscle's ability to create energy. At the cellular level, metabolic myopathies lack some kind of enzyme that prevent the chemical reactions necessary to create adenosine triphosphate (ATP). This prevents the muscle cells from being able to function properly and disrupts communication between joints and bones. Some people with a metabolic myopathy never develop symptoms due to the body's ability to produce enough ATP through alternative pathways. In the event more ATP is needed from the affected pathway, the lack of it becomes an issue and symptoms develop. People with a metabolic myopathy often experience symptoms such a

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  • اعتلال عضلي أيضي (ar)
  • Myopathie métabolique (fr)
  • Metabolic myopathy (en)
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  • الاعتلال العضلي الأيضي أو الاعتلال العضلي الاستقلابي (بالإنجليزية: Metabolic myopathy)‏ هو اعتلال عضلي ينتج عن خلل في الأيض الكيميائي الحيوي الذي يؤثر بشكل أولي على العضلات ومنها: * داء اختزان الغلايكوجين * * داء اختزان الفوسفات الكرياتيني (ar)
  • Les myopathies métaboliques sont les myopathies en rapport avec une anomalie de fonctionnement cellulaire des muscles chargée de produire l’énergie nécessaire au fonctionnement de ces muscles.Elles sont un sous-groupe des maladies neuromusculaires. (fr)
  • Metabolic myopathies are myopathies that result from defects in biochemical metabolism that primarily affect muscle. They are generally genetic defects that interfere with muscle's ability to create energy. At the cellular level, metabolic myopathies lack some kind of enzyme that prevent the chemical reactions necessary to create adenosine triphosphate (ATP). This prevents the muscle cells from being able to function properly and disrupts communication between joints and bones. Some people with a metabolic myopathy never develop symptoms due to the body's ability to produce enough ATP through alternative pathways. In the event more ATP is needed from the affected pathway, the lack of it becomes an issue and symptoms develop. People with a metabolic myopathy often experience symptoms such a (en)
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  • الاعتلال العضلي الأيضي أو الاعتلال العضلي الاستقلابي (بالإنجليزية: Metabolic myopathy)‏ هو اعتلال عضلي ينتج عن خلل في الأيض الكيميائي الحيوي الذي يؤثر بشكل أولي على العضلات ومنها: * داء اختزان الغلايكوجين * * داء اختزان الفوسفات الكرياتيني (ar)
  • Metabolic myopathies are myopathies that result from defects in biochemical metabolism that primarily affect muscle. They are generally genetic defects that interfere with muscle's ability to create energy. At the cellular level, metabolic myopathies lack some kind of enzyme that prevent the chemical reactions necessary to create adenosine triphosphate (ATP). This prevents the muscle cells from being able to function properly and disrupts communication between joints and bones. Some people with a metabolic myopathy never develop symptoms due to the body's ability to produce enough ATP through alternative pathways. In the event more ATP is needed from the affected pathway, the lack of it becomes an issue and symptoms develop. People with a metabolic myopathy often experience symptoms such as progressive muscle weakness, fatigue, pain and cramping after exercise, and considerable breakdown of muscle tissue. The degree of symptoms varies greatly from person to person and is dependent on the severity of enzymatic defect. In extreme cases it can lead to Rhabdomyolysis. (en)
  • Les myopathies métaboliques sont les myopathies en rapport avec une anomalie de fonctionnement cellulaire des muscles chargée de produire l’énergie nécessaire au fonctionnement de ces muscles.Elles sont un sous-groupe des maladies neuromusculaires. (fr)
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