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Anal Sphincter Myopathy, Internal
atrophic muscular disease +
Axial Myopathy, Late-Onset +
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia
Carey-Fineman-Ziter syndrome
Congenital Myopathy with Neuropathy and Deafness
Craniomandibular Disorders +
Early-Onset Myopathy with Fatal Cardiomyopathy
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2
eosinophilia-myalgia syndrome
Erythrocyte Amp Deaminase Deficiency
Erythrocyte Lactate Transporter Defect
familial periodic paralysis +
Fingerprint Body Myopathy
Gamstorp-Wohlfart syndrome
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis
Hypertrophia Musculorum Vera
Kocher-Debre-Semelaigne Syndrome
Late-Onset Carnitine Palmitoyltransferase II Deficiency
Marinesco-Sjogren syndrome
Medial Tibial Stress Syndrome
Mitochondrial DNA Depletion Syndrome, Myopathic Form +
Muscle Cramp + A sustained and usually painful contraction of muscle fibers. This may occur as an isolated phenomenon or as a manifestation of an underlying disease process (e.g., UREMIA; HYPOTHYROIDISM; MOTOR NEURON DISEASE; etc.). (From Adams et al., Principles of Neurology, 6th ed, p1398)
Muscular Hypoplasia, Congenital Universal, of Krabbe
myofascial pain syndrome +
Myopathic Carnitine Deficiency
Myopathy with Lactic Acidosis, Hereditary
Myopathy, Granulovacuolar Lobular, with Electrical Myotonia
MYOPATHY, SCAPULOHUMEROPERONEAL
myostatin-related muscle hypertrophy
neutral lipid storage disease +
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy
Pectoralis Muscle, Absence of
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss
Proximal Myopathy with Focal Depletion of Mitochondria
Singleton Merten Syndrome +
Skeletal Muscle Reperfusion Injury
systemic primary carnitine deficiency disease
Tel Hashomer Camptodactyly Syndrome
Treft Sanborn Carey Syndrome
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy
Uruguay Faciocardiomusculoskeletal Syndrome
very long chain acyl-CoA dehydrogenase deficiency
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