Structural and functional causes of hypernasality in velocardiofacial syndrome. A pilot study

Folia Phoniatr Logop. 2009;61(2):93-6. doi: 10.1159/000209252. Epub 2009 Mar 20.

Abstract

Objective: Hypernasality in velocardiofacial syndrome (VCFS) is more severe, persistent, and difficult to manage compared to other populations with cleft palate or velopharyngeal (VP) dysfunction. This pilot study investigated why children with VCFS have more severe hypernasality.

Methods: Pressure-flow methodology indirectly measured VP orifice size and VP closure timing during speech in a group of 5 children with VCFS, 5 children with cleft palate, and 6 normal children.

Results: Children with VCFS demonstrated significant differences in VP closure timing and hypernasality. There were no significant group differences in VP orifice size. Duration of nasal airflow was the strongest predictor of judgments of hypernasality.

Conclusion: This study provides preliminary evidence that VP closure timing may account for the more severe hypernasality in children with VCFS, compared to structural factors alone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Air Pressure
  • Child
  • Cleft Palate / complications
  • Cleft Palate / pathology
  • Cleft Palate / physiopathology
  • DiGeorge Syndrome / complications*
  • DiGeorge Syndrome / pathology
  • DiGeorge Syndrome / physiopathology*
  • Female
  • Humans
  • Linear Models
  • Male
  • Nose / physiopathology
  • Pilot Projects
  • Sound Spectrography
  • Speech
  • Speech Production Measurement
  • Transducers, Pressure
  • Velopharyngeal Sphincter / pathology
  • Velopharyngeal Sphincter / physiopathology
  • Voice Disorders / etiology*
  • Voice Disorders / pathology
  • Voice Disorders / physiopathology*
  • Voice Quality / physiology*