Abstract

H63D Syndrome Type-2 is a complex genetic disorder with diverse manifestations, including erratic iron metabolism, micro-inflammatory cascades, neuropsychiatric issues, organ damage, and other rare multi-faceted symptoms. A comprehensive understanding of the pathophysiology underlying this condition is essential for accurate diagnosis, appropriate management, and the development of targeted therapeutic approaches. Healthcare professionals should adopt a multidisciplinary approach to patient care and emphasize the importance of early detection, intervention, and patient education in the management of H63D Syndrome Type-2. Future research should focus on gene editing technologies and novel therapies to address the underlying genetic mutation and the diverse symptoms associated with the disorder.