Pitt-Hopkins Syndrome Awareness

This course provides an overview of Pitt Hopkins Syndrome, a rare genetic condition caused by mutation or deletion of the TCF4 gene. Delegates will gain knowledge of the syndrome’s genetic basis, clinical and physical characteristics, and its impact on daily living. The session explores practical interventions to support individuals living with the condition, with emphasis on person-centred care, family involvement, and multi-disciplinary support. This course is ideal for healthcare staff, educators, and support workers supporting those with rare neurodevelopmental disorders.