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Results 11 - 20 of 32 for Progressive peripheral neuropathy
  1. BSCL2 gene 
    ... the severe neurological problems seen in children with progressive encephalopathy with or without lipodystrophy. ... EB, Robl T, Hartl G, Hartung HP, Wagner K, Windpassinger C; Austrian Peripheral Neuropathy Study Group. Phenotypes of the N88S Berardinelli-Seip ...
    https://medlineplus.gov/genetics/gene/bscl2 - Genetics
  2. Autosomal recessive axonal neuropathy with neuromyotonia 
    ... caused by damage to a particular part of peripheral nerves called axons, which ... causes progressive weakness and wasting (atrophy) of muscles in the ...
    https://medlineplus.gov/...sive-axonal-neuropathy-with-neuromyotonia - Genetics
  3. Troyer syndrome 
    ... spinal cord to the rest of the body (peripheral neuropathy). Troyer syndrome ... and talk, progressive weakness and spasticity of the leg muscles, muscle ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  4. Andermann syndrome 
    ... callosum with neuronopathy Agenesis of corpus callosum with peripheral neuropathy Agenesis of corpus callosum with polyneuropathy Charlevoix disease ... Testing Registry: Agenesis of the corpus callosum with peripheral neuropathy Corpus callosum agenesis-neuronopathy syndrome National Organization for ...
    https://medlineplus.gov/genetics/condition/andermann-syndrome - Genetics
  5. Action myoclonus–renal failure syndrome 
    ... loss of sensation and weakness in the limbs (peripheral neuropathy), or hearing loss caused by abnormalities in the ... syndrome Action myoclonus–renal failure syndrome AMRF Epilepsy, progressive myoclonic 4, with or without renal failure EPM4 ...
    https://medlineplus.gov/.../action-myoclonus-renal-failure-syndrome - Genetics
  6. Combined oxidative phosphorylation deficiency 1 
    ... delay, seizures, loss of sensation in the limbs (peripheral neuropathy), and an unusually small head (microcephaly). Liver disease ... and symptoms of the condition. COXPD1 Early fatal progressive hepatoencephalopathy Hepatoencephalopathy due to combined oxidative phosphorylation defect ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  7. Spinocerebellar ataxia type 3 
    ... loss of sensation and weakness in the limbs (peripheral neuropathy), muscle cramps, muscle twitches (fasciculations), and swallowing difficulties. ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  8. Spinocerebellar ataxia type 2 
    ... loss of sensation and weakness in the limbs (peripheral neuropathy), muscle wasting (atrophy), uncontrolled muscle tensing (dystonia), and ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  9. OPA1 gene 
    ... loss of sensation and weakness in the limbs (peripheral neuropathy), difficulty coordinating movements (ataxia), feeding and digestive difficulties, ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  10. HSPB1 gene 
    ... Timmerman V. Small heat shock proteins in inherited peripheral neuropathies. Ann Med. 2005;37(6):413-22. doi: ...
    https://medlineplus.gov/genetics/gene/hspb1 - Genetics
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