Keywords:
CDKL5 deficiency disorder; Developmental epileptic encephalopathy; Gross motor function; Psychometric properties
Abstract:
Validated measures capable of demonstrating meaningful interventional change in the CDKL5 deficiency disorder (CDD) are lacking. The study objective was to modify the Rett Syndrome Gross Motor Scale (RSGMS) and evaluate its psychometric properties for individuals with CDD.