Muscle dystrophies
|
Duchenne and Becker muscular dystrophies |
Dystrophin mutations in female carriers |
Limb girdle |
Myofibrillar myopathy |
Desmin-related myofibrillar myopathy |
Myotonic dystrophy |
Metabolic and mitochondrial disorders of muscle
|
Carnitine palmitoyltransferase II deficiency |
McArdle disease |
Myoadenylate deaminase deficiency |
Mitochondrial myopathies |
Pompe disease (acid maltase deficiency) |
Inflammatory myopathies
|
Hypomyopathic dermatomyositis |
Inclusion body myositis |
Clinically amyopathic dermatomyositis |
Antisynthetase syndrome |
Others
|
Familial elevated creatine kinase |
Sarcoid myopathy |
Motor neuron diseases |
Charcot-Marie-Tooth disease |
Other congenital diseases |