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

Abstract 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.

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Autores principales:	Ratna Acharya, Kiran Upadhyay
Formato:	article
Lenguaje:	EN
Publicado:	Wiley 2021
Materias:	child focal segmental glomerulosclerosis nephrotic syndrome NUP93 Medicine R Medicine (General) R5-920
Acceso en línea:	https://doaj.org/article/e7c0abb46284435dbf8281afd03d3f17
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spelling	oai:doaj.org-article:e7c0abb46284435dbf8281afd03d3f172021-12-01T06:36:08ZEnd‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant2050-090410.1002/ccr3.5111https://doaj.org/article/e7c0abb46284435dbf8281afd03d3f172021-11-01T00:00:00Zhttps://doi.org/10.1002/ccr3.5111https://doaj.org/toc/2050-0904Abstract 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.Ratna AcharyaKiran UpadhyayWileyarticlechildfocal segmental glomerulosclerosisnephrotic syndromeNUP93MedicineRMedicine (General)R5-920ENClinical Case Reports, Vol 9, Iss 11, Pp n/a-n/a (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	child focal segmental glomerulosclerosis nephrotic syndrome NUP93 Medicine R Medicine (General) R5-920
spellingShingle	child focal segmental glomerulosclerosis nephrotic syndrome NUP93 Medicine R Medicine (General) R5-920 Ratna Acharya Kiran Upadhyay End‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant
description	Abstract 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.
format	article
author	Ratna Acharya Kiran Upadhyay
author_facet	Ratna Acharya Kiran Upadhyay
author_sort	Ratna Acharya
title	End‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant
title_short	End‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant
title_full	End‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant
title_fullStr	End‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant
title_full_unstemmed	End‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant
title_sort	end‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous nup93 variant
publisher	Wiley
publishDate	2021
url	https://doaj.org/article/e7c0abb46284435dbf8281afd03d3f17
work_keys_str_mv	AT ratnaacharya endstagerenaldiseaseinachildwithfocalsegmentalglomerulosclerosisassociatedwithahomozygousnup93variant AT kiranupadhyay endstagerenaldiseaseinachildwithfocalsegmentalglomerulosclerosisassociatedwithahomozygousnup93variant
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End‐stage renal disease in a child with focal segmental glomerulosclerosis associated with a homozygous NUP93 variant

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