Audiological findings in Noonan syndrome

Tokgoz-Yilmaz S., TÜRKYILMAZ M. D., Cengiz F. B., Sjostrand A. P., KÖSE S. K., Tekin M.

International Journal of Pediatric Otorhinolaryngology, cilt.89, ss.50-54, 2016 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 89
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1016/j.ijporl.2016.07.031
  • Dergi Adı: International Journal of Pediatric Otorhinolaryngology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.50-54
  • Anahtar Kelimeler: Noonan syndrome, Hearing loss, Transient otoacoustic emissions, TURNER-PHENOTYPE, PTPN11 GENE, MUTATIONS, DISORDERS, CHILDREN, GROWTH, FAMILY
  • Ankara Üniversitesi Adresli: Evet

Özet

© 2016 Elsevier Ireland LtdObjectives The aim of this study was to evaluate audiologic properties of patients with Noonan syndrome and compare these findings with those of unaffected peers. Methods The study included 17 children with Noonan syndrome and 20 typically developing children without Noonan syndrome. Pure tone and speech audiometry, immitancemetric measurement, otoacoustic emissions measurement and auditory brainstem response tests were applied to all (n = 37) children. Results Hearing thresholds of children with Noonan syndrome were higher (poorer) than those observed unaffected peers, while the hearing sensitivity of the both groups were normal limits (p = 0.013 for right, p = 0.031 for left ear). Transient evoked otoacoustic emissions amplitudes of the children with Noonan syndrome were lower than the children without Noonan syndrome (p = 0.005 for right, p = 0.002 for left ear). Middle ear pressures and auditory brainstem response values were within normal limits and there was no difference between the two groups (p > 0.05). Conclusion General benefit of the present study is to characterize the audiologic findings of children with Noonan syndrome, which is beneficial in clinics evaluating children with Noonan syndrome.