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Article

Familial focal segmental glomerulosclerosis: mutation in inverted formin 2 mimicking Alport syndrome.

The Netherlands journal of medicine - 1 Feb 2016

Rood I M, Bongers E M H F, Lugtenberg D, Klein I H H T, Steenbergen E J, Wetzels J F M, Deegens J K J

Abstract excerpt

Focal segmental glomerulosclerosis (FSGS) is one of the most common patterns of glomerular injury. FSGS can be caused by mutations in genes encoding proteins that play key roles in the function of the podocyte and glomerular basement membrane. In this case report we present a family with FSGS initially suspected to be Alport syndrome. Genetic analysis according to the Dutch guidelines of FSGS revealed a mutation...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Glomerulosclerosis, Focal Segmental

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Source

Identifiers

PMID: 26951353

Genes

INF2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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