Discover Community Create You

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

Familial FSGS.

Advances in chronic kidney disease - 1 Sept 2014

Pollak Martin R

Abstract excerpt

Focal segmental glomerulosclerosis (FSGS) and nephrotic syndrome can be caused by rare highly penetrant mutations in number of genes. FSGS can follow both recessive and dominant inheritance patterns. In general, recessive forms present early, whereas the autosomal dominant forms present in adolescence or adulthood. Many of the genes found to be mutated in FSGS and nephrotic syndrome patients encode proteins...

Read the complete abstract on PubMed

Topics

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

Share to Apolipoprotein L1
Share to Apolipoproteins
Share to Black People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to APOL1 gene

Share to Genetic Predisposition to Disease

Share to Glomerulosclerosis, Focal Segmental

Share to Lipoproteins, HDL

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 25168831
DOI: 10.1053/j.ackd.2014.06.001
PMCID: PMC4197186

Genes

APOL1

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial FSGS.PMID 25168831Read ↗

A Review of Focal Segmental Glomerulosclerosis Classification With a Focus on Genetic AssociationsSemantic proximity Read ↗

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

Familial forms of nephrotic syndrome.Semantic proximity Read ↗

A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis.Semantic proximity Read ↗

Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism.Semantic proximity Read ↗

LAMA2 and LOXL4 Are Candidate FSGS GenesSemantic proximity Read ↗

Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.Semantic proximity Read ↗

Familial focal segmental glomerulosclerosis (FSGS) in a Nigerian family and exclusion of mutations in NPHS2,WT1 and APOL1.Semantic proximity Read ↗

Genetic causes of focal segmental glomerulosclerosis: implications for clinical practice.Semantic proximity Read ↗

Monogenic focal segmental glomerulosclerosis: A conceptual framework for identification and management of a heterogeneous diseaseSemantic proximity Read ↗

Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis.Semantic proximity Read ↗

Focal and segmental glomerulosclerosis.Semantic proximity Read ↗

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