This report presents key insights from the 2022 annual conference held in Edinburgh, commemorating the 10th anniversary of the discovery of ATP1A3 variants in alternating hemiplegia of childhood (AHC). This milestone event marked a decade of rapid advancements in research and clinical understanding, bringing together international experts and those with lived experience to reflect on progress, identify ongoing challenges, and shape the future of ATP1A3-related disease research.
Link: https://pmc.ncbi.nlm.nih.gov/articles/PMC12488843/
Alternating Hemiplegia of Childhood and ATP1A3-Related Diseases: Insights From a Decade of Discovery and Collaboration.
Simpson AJ, McLellan A, Behl KE, Brown J, Clapcote SJ, Cross JH, van den Maagdenberg AMJM, Vezyroglou AN, Balestrini S, Sisodiya SM. Neurol Genet. 2025 Sep 30;11(5):e200308
