Case report
Open access
Aug 2026
A novel TRPC6 variant (c.131C>T, p.(Pro44Leu)) associated with focal segmental glomerulosclerosis: a case report
This case demonstrates that genetic testing can guide personalized management in young patients with FSGS, offering a practical framework for avoiding unnecessary treatment-related morbidity and highlights the value of early supportive therapy in genetic FSGS.
Fan Yang, Xiao-Qi Wang, Yan Li et al.
· Frontiers in Genetics · 0 citations