September 7 - September 9
Many genetic causes of neurodevelopmental disorders have been elucidated in the last decade. A substantial proportion of the causative genes cluster in the chromatin remodeling pathway. The aim of this conference is to highlight the common pathways involved in multiple chromatin remodeling disorders as well as to provide participants with an overview of the methodologies in this rapidly expanding field of epigenetic research. This meeting will bring together scientists and clinicians involved in genetic disease identification, characterization and treatment, as well as those involved in the development of epigenetic methodology. The scientific conference will be completed by a patient community gathering of families with the Helsmoortel – Van der Aa syndrome, a leading cause of syndromic autism due to mutations in ADNP.