Neuromuscular Disorders

Related topics on Genetics Home Reference:

• amyotrophic lateral sclerosis
• Andermann syndrome
• ataxia with vitamin E deficiency
• central core disease
• Charcot-Marie-Tooth disease
• distal hereditary motor neuropathy, type V
• Duchenne and Becker muscular dystrophy
• Emery-Dreifuss muscular dystrophy
• facioscapulohumeral muscular dystrophy
• familial dysautonomia
• Fukuyama congenital muscular dystrophy
• giant axonal neuropathy
• hereditary neuralgic amyotrophy
• hereditary neuropathy with liability to pressure palsies
• hyperkalemic periodic paralysis
• hypokalemic periodic paralysis
• inclusion body myopathy 2
• inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
• infantile-onset ascending hereditary spastic paralysis
• juvenile primary lateral sclerosis
• L1 syndrome
• Laing distal myopathy
• mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
• multiminicore disease
• myostatin-related muscle hypertrophy
• myotonia congenita
• myotonic dystrophy
• neurofibromatosis type 1
• neuropathy, ataxia, and retinitis pigmentosa
• oculopharyngeal muscular dystrophy
• paramyotonia congenita
• Pelizaeus-Merzbacher disease
• potassium-aggravated myotonia
• spastic paraplegia type 11
• spastic paraplegia type 2
• spastic paraplegia type 3A
• spastic paraplegia type 4
• spastic paraplegia type 7
• spastic paraplegia type 8
• spinal and bulbar muscular atrophy
• spinal muscular atrophy
• Tangier disease
• tibial muscular dystrophy
• transthyretin amyloidosis
• Troyer syndrome
• X-linked myotubular myopathy

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