Now showing items 1-2 of 2
Variations in Craniofacial and Velopharyngeal Structures Among Individuals with 22q11.2 Deletion Syndrome
(East Carolina University, 2016-07-25)
22q11.2 deletion syndrome is the most common genetic cause of velopharyngeal dysfunction. Studies examining 22q11.2 deletion syndrome have thus far primarily focused on variations in the bony framework. Limited information ...
PREDICTING VELOPHARYNGEAL CLOSURE PATTERNS BASED ON ANATOMIC VARIABLES
(East Carolina University, 2016-04-14)
Objective: The purpose of this study is to examine the effects of velopharyngeal (VP) variables and sex among adults with normal velopharyngeal anatomy to determine if these variables could correspond with VP closure ...