Utility of 3D-Gait Analysis for planning Rehabilitation Program for an 8-Year-Old Child Diagnosed with KBG Syndrome: A Case Report

KBG syndrome (ICD-10: Q87.8) is a rare genetic condition resulting from mutations in the ANKRD11 gene, characterized by distinctive facial features, macrodontia, skeletal anomalies, and developmental delays. An 8-year-old male child with KBG syndrome presented with an abnormal gait pattern. The child was enrolled for gait analysis using the Qualysis motion capture system for detailed objective gait evaluation, like spatiotemporal and kinematic parameters . This report demonstrates the utility of detailed preoperative gait analysis for informed clinical decision-making, coordinated rehabilitation planning, and the development of structured prehabilitation strategies.