The goals of the 2024 conference are:
- To provide an educational experience by sharing the most recent advances in diagnosis, treatments and management of SMS throughout the lifespan.
- To facilitate family-to-family support, prioritizing time to interact, network and discuss issues regarding SMS.
- To recognize the psychosocial aspects impacting SMS families and the role of PRISMS as a network.
- To bring together families and professionals to foster partnerships to advance the awareness and understanding of Smith-Magenis syndrome.