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End-stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant.

Ratna AcharyaKiran K Upadhyay
Published 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.
Keyphrases
  • end stage renal disease
  • chronic kidney disease
  • peritoneal dialysis
  • genome wide
  • copy number
  • mental health
  • dna methylation
  • free survival
  • genome wide identification
  • transcription factor