Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome.

Fetal and pediatric pathology - 1 Apr 2021

Karmila A B, Yap Y C, Appadurai M, Oh L, Fazarina M, Abd Ghani F, Ariffin H

Abstract excerpt

Introduction: Denys-Drash Syndrome (DDS) consists of a triad of pseudohermaphroditism, Wilms'tumor and nephropathy. This condition may manifest as a complete triad or in an incomplete form; with either one or a combination of the above features. The characteristic glomerular abnormality in DDS is diffuse mesangial sclerosis (DMS).Case report: We report two cases of DDS with focal membranoproliferative...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child, Preschool
Share to Genes, Wilms Tumor
Share to Glomerulonephritis, Membranoproliferative

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kidney Diseases

Share to Mutation

Share to Nephrotic Syndrome

Share to Wilms Tumor

Share to WT1 Proteins

Source

Identifiers

PMID: 31707902
DOI: 10.1080/15513815.2019.1686788

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Focal Segmental Membranoproliferative Glomerulonephritis: A Histological Variant of Denys-Drash Syndrome.PMID 31707902Read ↗

WT1-related disorders: more than Denys-Drash syndrome.Semantic proximity Read ↗

[Clinical and pathological features of Denys-Drash syndrome: report of 3 cases].Semantic proximity Read ↗

WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review.Semantic proximity Read ↗

WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia.Semantic proximity Read ↗

Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report.Semantic proximity Read ↗

A familial WT1 mutation associated with incomplete Denys-Drash syndrome.Semantic proximity Read ↗

WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerular sclerosis with embryonal hyperplasiaSemantic proximity Read ↗

A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis.Semantic proximity Read ↗

Clinical spectrum of Denys-Drash and Frasier syndrome.Semantic proximity Read ↗

A Case of UMOD-Associated Nephropathy Mimicking Focal Segmental Glomerulosclerosis in a Young Male with a Positive Family HistorySemantic proximity Read ↗

WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis.Semantic proximity Read ↗

Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adultsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.