Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysis.

Objective: 22q11.2 deletion syndrome is the most common genetic cause of velopharyngeal dysfunction (VPD). Magnetic resonance imaging (MRI) is a promising method for noninvasive, three-dimensional (3D) assessment of velopharyngeal (VP) anatomy. The purpose of this study was to assess VP structure in...

Full description

Bibliographic Details

Published in:	Cleft Palate Craniofacial Journal Vol. 43; no. 4; pp. 446 - 457
Main Authors:	Ruotolo RA, Veitia NA, Corbin A, McDonough J, Solot CB, McDonald-McGinn D, Zackai EH, Emanuel BS, Cnaan A, LaRossa D, Arens R, Kirschner RE
Format:	pictorial research tables/charts Journal Article
Published:	Sage Publications Inc. Jul2006
Online Access:	View this record in EBSCOhost