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.
CITATION STYLE
Acharya, R., & Upadhyay, K. (2021). End-stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant. Clinical Case Reports, 9(11). https://doi.org/10.1002/ccr3.5111
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