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Results 1 - 10 of 10 for Abnormal demyelination
  1. Fatty acid hydroxylase-associated neurodegeneration 
    ... of this enzyme's function may result in abnormal myelin that is prone to deterioration (demyelination), leading to a loss of white matter (leukodystrophy). ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  2. FA2H gene 
    ... of this enzyme's function may result in abnormal myelin that is prone to deterioration (demyelination), leading to a loss of white matter (leukodystrophy). ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics
  3. Krabbe disease 
    ... leukodystrophies, which result from the loss of myelin (demyelination) in the nervous system. Myelin is the protective covering around nerve cells that ensures the rapid transmission of nerve signals. Krabbe disease is also characterized by abnormal cells in the brain called globoid cells, which ...
    https://medlineplus.gov/genetics/condition/krabbe-disease - Genetics
  4. Peroxisomal acyl-CoA oxidase deficiency 
    ... CoA oxidase deficiency. However, researchers suggest that the abnormal fatty acid accumulation triggers inflammation in the nervous ...
    https://medlineplus.gov/.../peroxisomal-acyl-coa-oxidase-deficiency - Genetics
  5. LMNB1 gene 
    ... In people with ADLD, the loss of myelin (demyelination) occurs in the brain and spinal cord (central nervous system), often years before movement problems develop. Demyelination of the spinal cord likely contributes to the ...
    https://medlineplus.gov/genetics/gene/lmnb1 - Genetics
  6. Autosomal dominant leukodystrophy with autonomic disease 
    ... and maintenance over time.The loss of myelin (demyelination) occurs in the brain and spinal cord (central ... with ADLD, often years before movement problems develop. Demyelination of the spinal cord likely contributes to the ...
    https://medlineplus.gov/...ant-leukodystrophy-with-autonomic-disease - Genetics
  7. PMP22 gene 
    ... activities, leading to instability and loss of myelin (demyelination). Demyelination reduces the ability of the peripheral nerves to ... normal functions of the Schwann cell, leading to demyelination and producing the signs and symptoms of CMT1A. ...
    https://medlineplus.gov/genetics/gene/pmp22 - Genetics
  8. Yuan-Harel-Lupski syndrome 
    ... protein leads to instability and loss of myelin (demyelination). Demyelination reduces the ability of the peripheral nerves to ...
    https://medlineplus.gov/.../condition/yuan-harel-lupski-syndrome - Genetics
  9. Chromosome 17 
    ... and lead to instability and loss of myelin (demyelination). Shortage and dysfunction of myelin reduce the ability ... abnormality causes severe intellectual disability, developmental delay, seizures, abnormal muscle stiffness (spasticity), weak muscle tone (hypotonia), and ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  10. Alpha-mannosidosis 
    ... alpha-mannosidosis: clinical progression in the absence of demyelination. Neurology. 2004 Nov 9;63(9):1744-6. ...
    https://medlineplus.gov/genetics/condition/alpha-mannosidosis - Genetics