End-stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant.
Ratna AcharyaKiran K UpadhyayPublished in: Clinical case reports (2021)
This report highlights that the genetic causes of FSGS, including NUP93 gene variant, such as the one described in this report, progress to end-stage renal disease rapidly and that the risk of recurrence post-renal transplantation is less likely.