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Results 1 - 10 of 37 for Motor neuron disease
  1. Amyotrophic lateral sclerosis 
    ... Dementia with amyotrophic lateral sclerosis Lou Gehrig disease Motor neuron disease, amyotrophic lateral sclerosis Genetic Testing Registry: Amyotrophic lateral ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  2. Riboflavin transporter deficiency neuronopathy 
    ... reveals riboflavin transporter mutations as a cause of motor neuron disease. Brain. 2012 Sep;135(Pt 9):2875-82. ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  3. Sandhoff disease 
    ... of juvenile-onset Sandhoff disease presenting with a motor neuron disease phenotype and a novel variant. Brain Dev. 2021 ...
    https://medlineplus.gov/genetics/condition/sandhoff-disease - Genetics
  4. Distal hereditary motor neuropathy, type V 
    ... Suzuki N. Molecular pathogenesis of seipin/BSCL2-related motor neuron diseases. Ann Neurol. 2007 Mar;61(3):237-50. ...
    https://medlineplus.gov/...distal-hereditary-motor-neuropathy-type-v - Genetics
  5. Troyer syndrome 
    ... syndrome: a combination of central brain abnormality and motor neuron disease? J Neurol. 1999 Jul;246(7):556-61. ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  6. Spinal muscular atrophy 
    ... Other forms of spinal muscular atrophy and related motor neuron diseases, such as spinal muscular atrophy with progressive myoclonic ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  7. Spastic paraplegia type 49 
    ... of TECPR2 in a complex form of progressive motor neuron disease. Clin Genet. 2016 Aug;90(2):182-5. ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-49 - Genetics
  8. Autosomal recessive cerebellar ataxia type 1 
    ... Kawakami H. Cerebellar ataxia with SYNE1 mutation accompanying motor neuron disease. Neurology. 2013 Feb 5;80(6):600-1. ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  9. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... disease of bone and/or frontotemporal dementia Lower motor neuron degeneration with Paget-like bone disease Multisystem proteinopathy Muscular dystrophy, limb-girdle, with Paget ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  10. Spinal and bulbar muscular atrophy 
    ... and bulbar muscular atrophy, also known as Kennedy disease, is a disorder of specialized nerve cells that control muscle movement (motor neurons). These nerve cells originate in the spinal cord ...
    https://medlineplus.gov/.../spinal-and-bulbar-muscular-atrophy - Genetics
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