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Central motor and sensory conduction in X-linked recessive bulbospinal neuronopathy.
  1. T Kachi,
  2. G Sobue,
  3. I Sobue
  1. Department of Neurology, Chubu National Hospital, Obu, Japan.

    Abstract

    Central conduction was studied in 12 patients with X-linked recessive bulbospinal neuronopathy (XBSN) using percutaneous electrical cortical, cervical and lumbar stimulation and somatosensory evoked potentials (SEPs). The central motor conduction time from the motor cortex to the cervical and lumbar segments of the spinal cord was normal in XBSN. SEPs, however, were abnormal or central sensory conduction time was prolonged in patients with XBSN. These results are consistent with the clinicopathological findings of XBSN in which the primary sensory neurons are involved as well as the lower motor neurons in the CNS, whereas the upper motor neurons are well preserved.

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