Basic Science
Children with Chronic Conditions
Clinical Research
Nephrology
Kandai Nozu, MD, PhD (he/him/his)
Professor
Kobe University Graduate School of Medicine
Kobe, Hyogo, Japan
Session
Description: Genetic and genomic studies have the potential to provide important new insights into the mechanisms of renal disease and to identify new therapeutic targets.
Approximately 90% of the patients with childhood-onset nephrotic syndrome are idiopathic of unknown etiology. Advances in genetics have identified single-gene abnormalities in some cases of congenital nephrotic syndrome, infantile nephrotic syndrome, and steroid-resistant nephrotic syndrome. And disease susceptibility genes have also been identified in steroid-sensitive nephrotic syndrome, considered a multi-factorial genetic disease. We are entering a new phase in developing personalized medicine now.
In this symposium, we would like to deepen our understanding of the latest knowledge, the discovery process, and the possibility of applying it to new treatments for nephrotic syndrome in the future.
Speaker: Jiwon M. Lee, MDPhD (she/her/hers) – Korea Disease Control and Prevention Agency (Korea CDC)
Speaker: Yutaka Harita, MD, PhD – The University of Tokyo
Speaker: Michelle T. McNulty, MS (she/her/hers) – Boston Children's Hospital
Speaker: Tomoko Horinouchi, MD,PhD – Kobe University Graduate School of Medicine