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Results 1 - 7 of 7 for Corticospinal tract hypoplasia
  1. Hypomyelination with brainstem and spinal cord involvement and leg spasticity 
    ... seen using magnetic resonance imaging (MRI). These characteristic abnormalities typically involve specific regions (called tracts) within the brainstem and spinal cord, especially the pyramidal tract, lateral corticospinal tract, and the dorsal column. HBSL ...
    https://medlineplus.gov/...pinal-cord-involvement-and-leg-spasticity - Genetics
  2. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... seen using magnetic resonance imaging (MRI). These characteristic abnormalities ... the pyramidal tract and the dorsal column. In addition, most affected ...
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics
  3. L1 syndrome 
    ... paraplegia type 1 do not usually have major abnormalities in structures of the brain.X-linked complicated corpus callosum agenesis is defined by underdevelopment (hypoplasia) or absence (agenesis) of the tissue that connects ...
    https://medlineplus.gov/genetics/condition/l1-syndrome - Genetics
  4. ATL1 gene 
    ... cells (neurons) that extend down the spinal cord (corticospinal tracts). These neurons send electrical signals that lead to ... of axons. Within the long neurons of the corticospinal tracts, these problems can lead to cell death. As ...
    https://medlineplus.gov/genetics/gene/atl1 - Genetics
  5. LMNB1 gene 
    ... nerve cells that extend down the spinal cord (corticospinal tracts) and control voluntary muscle movement. More About This ...
    https://medlineplus.gov/genetics/gene/lmnb1 - Genetics
  6. Autosomal dominant leukodystrophy with autonomic disease 
    ... nerve cells that extend down the spinal cord (corticospinal tracts) and control voluntary muscle movement. LMNB1 This condition ...
    https://medlineplus.gov/...ant-leukodystrophy-with-autonomic-disease - Genetics
  7. Fatty acid hydroxylase-associated neurodegeneration 
    ... development of the movement problems and other neurological abnormalities that occur in FAHN. Iron accumulation in the ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics