Deficient auditory interhemispheric transfer in patients with PAX6 mutations

Doris Eva Bamiou, Frank E. Musiek, Sanjay M. Sisodiya, Samantha L. Free, Rosalyn A. Davies, Anthony Moore, Veronica Van Heyningen, Linda M. Luxon

Research output: Contribution to journalArticle

31 Scopus citations

Abstract

PAX6 mutations are associated with absence/hypoplasia of the anterior commissure and reduction in the callosal area in humans. Both of these structures contain auditory interhemispheric fibers. The aim of this study was to characterize central auditory function in patients with a PAX6 mutation. We conducted central auditory tests (dichotic speech, pattern, and gaps in noise tests) on eight subjects with a PAX6 mutation and eight age- and sex-matched controls. Brain magnetic resonance imaging showed absent/hypoplastic anterior commissure in six and a hypoplastic corpus callosum in three PAX6 subjects. The control group gave normal central auditory tests results. All the PAX6 subjects gave abnormal results in at least two tests that require interhemispheric transfer, and all but one gave normal results in a test not requiring interhemispheric transfer. The left ear scores in the dichotic speech tests was significantly lower in the PAX6 than in the control group. These results are consistent with deficient auditory interhemispheric transfer in patients with a PAX6 mutation, which may be attributable to structural and/or functional abnormalities of the anterior commisure and corpus callosum, although the exact contribution of these two formations to our findings remains unclear. Our unique findings broaden the possible functions of PAX6 to include neurodevelopmental roles in higher order auditory processing.

Original languageEnglish (US)
Pages (from-to)503-509
Number of pages7
JournalAnnals of Neurology
Volume56
Issue number4
DOIs
StatePublished - Oct 2004

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Fingerprint Dive into the research topics of 'Deficient auditory interhemispheric transfer in patients with PAX6 mutations'. Together they form a unique fingerprint.

  • Cite this

    Bamiou, D. E., Musiek, F. E., Sisodiya, S. M., Free, S. L., Davies, R. A., Moore, A., Van Heyningen, V., & Luxon, L. M. (2004). Deficient auditory interhemispheric transfer in patients with PAX6 mutations. Annals of Neurology, 56(4), 503-509. https://doi.org/10.1002/ana.20227