Auditory function in Pelizaeus-Merzbacher disease

J Neurol. 2018 Jul;265(7):1580-1589. doi: 10.1007/s00415-018-8884-x. Epub 2018 May 3.

Abstract

Pelizaeus-Merzbacher disease (PMD; MIM 312080), an inherited defect of central nervous system myelin formation, affects individuals in many ways, including their hearing and language abilities. The aim of this study was to assess the auditory abilities in 18 patients with PMD by examining the functional processes along the central auditory pathways using auditory brainstem responses (ABR) and cortical auditory evoked potentials (CAEP) in response to speech sounds. The significant ABR anomalies confirm the existence of dyssynchrony previously described at the level of the brainstem in patients with PMD. Despite the significant auditory dyssynchrony observed at the level of the brainstem, CAEPs were present in most patients, albeit somehow abnormal in terms of morphology and latency, resembling a type of auditory neuropathy spectrum disorder.

Keywords: Auditory brainstem responses; Cortical auditory evoked potentials; Hearing; Pelizaeus–Merzbacher disease.

MeSH terms

  • Acoustic Impedance Tests
  • Acoustic Stimulation
  • Adolescent
  • Adult
  • Auditory Diseases, Central / diagnosis
  • Auditory Diseases, Central / etiology*
  • Auditory Diseases, Central / pathology
  • Auditory Pathways / physiopathology
  • Child
  • Child, Preschool
  • Electroencephalography
  • Evoked Potentials, Auditory, Brain Stem / physiology*
  • Female
  • Humans
  • Infant
  • Male
  • Otoacoustic Emissions, Spontaneous
  • Otoscopy
  • Pelizaeus-Merzbacher Disease / complications*
  • Young Adult