Rare kidney disease research, genomics and registry data will be in focus at the Alport Research Hub Symposium 2026 on 3 July.

The symposium brings together leading researchers and clinicians working in Alport syndrome, including several UKKA members and collaborators involved in RaDaR, the UK National Registry of Rare Kidney Diseases.

The programme is chaired by Professor Daniel Gale, Chair of RaDaR, and includes presentations from UKKA and RaDaR researchers, including Dr Katie Wong, who will present new longitudinal analysis from more than 1,000 RaDaR Alport patients exploring how genotype may influence disease severity and progression.