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Article

NPHS2 mutation associated with recurrence of proteinuria after transplantation.

Pediatric nephrology (Berlin, Germany) - 1 May 2004

Billing Heiko, Müller Dominik, Ruf Rainer, Lichtenberger Anne, Hildebrandt Friedhelm, August Christian, Querfeld Uwe, Haffner Dieter

Abstract excerpt

Mutations in the NPHS2 gene encoding podocin are associated with steroid-resistant nephrotic syndrome (SRNS) in childhood. Patients usually present with focal segmental glomerulosclerosis (FSGS). It is unclear to what extent SRNS due to NPHS2 mutations predisposes to recurrence of proteinuria/FSGS after renal transplantation (RTx). A 4-year-old girl with infantile SRNS was started on peritoneal dialysis because...

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Share to Anti-Inflammatory Agents
Share to Chromosomes, Human, Pair 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glomerulosclerosis, Focal Segmental

Share to Kidney Failure, Chronic

Share to Kidney Transplantation

Share to Methylprednisolone

Share to Nephrotic Syndrome

Share to Proteinuria

Source

Identifiers

PMID: 15015071
DOI: 10.1007/s00467-003-1408-6

Genes

NPHS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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NPHS2 mutation associated with recurrence of proteinuria after transplantation.PMID 15015071Read ↗

Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.Semantic proximity Read ↗

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Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.Semantic proximity Read ↗

Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation.Semantic proximity Read ↗

Post-Transplant Recurrence of Focal Segmental Glomerulosclerosis in a Child With Heterozygous Mutations in NPHS1 and NPHS2.Semantic proximity Read ↗

The podocin mutation R229Q and early recurrence (within the first year) of glomerular disease after renal transplantation.Semantic proximity Read ↗

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.Semantic proximity Read ↗

Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.Semantic proximity Read ↗

Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.Semantic proximity Read ↗

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.Semantic proximity Read ↗

NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.Semantic proximity Read ↗

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