Myofibrillar myopathy
MONDO:0018943Myofibrillar myopathy (MFM) describes a group of skeletal and cardiac muscle disorders, defined by the disintegration of myofibrils and aggregation of degradation products into intracellular inclusions, and is typically clinically characterized by slowly-progressive muscle weakness, which initially involves the distal muscles, but is highly variable and that can affect the proximal muscles as well as the cardiac and respiratory muscles in some patients.
Also known as: myofibrillar myopathy, myofibrillar myopathy (disease), Alpha Beta crystallinopathy (type), Desminopathy (type), Protein surplus myopathy (former name), Zaspopathy (type), desmin related myopathy (former name), desmin storage myopathy (former name)
6 clinical trials for this condition and its sub-types, 1 tagged with Myofibrillar myopathy itself.
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Browse by category āSub-types of Myofibrillar myopathy
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Central core myopathy 2 trials
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Myofibrillar myopathy 1 0 trials
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Myofibrillar myopathy 10 0 trials
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Myofibrillar myopathy 11 0 trials
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Myofibrillar myopathy 3 0 trials
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Myofibrillar myopathy 4 0 trials
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Myofibrillar myopathy 5 0 trials
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Myofibrillar myopathy 6 0 trials
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Myofibrillar myopathy 7 0 trials
1 sub-type
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Myofibrillar myopathy 8 0 trials