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Article

[Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy].

Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft - 1 Mar 2008

Müller M, Kusserow C, Orth U, Klär-Dissars U, Laqua H, Gal A

Abstract excerpt

PURPOSE: Autosomal dominant (familial) exudative vitreoretinopathy (adEVR) is a rare, congenital disease of the retinal vascular system, which may lead to blindness in severely affected eyes. One of the causative disease genes is located on chromosome 11q13-q23 and codes for "frizzled-4" (FZD4),...

Read the complete abstract on PubMed

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Share to Chromosomes, Human, Pair 11
Share to Exudates and Transudates
Share to Fluorescein Angiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Frizzled Receptors

Share to Genes, Dominant

Share to Receptors, G-Protein-Coupled

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Source

Identifiers

PMID: 17899116
DOI: 10.1007/s00347-007-1617-7

Genes

FZD4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17899116-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Research trail→

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[Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy].PMID 17899116Read ↗

A novel variant in the FZD4 gene leading to familial exudative vitreoretinopathy: A case report and literature review.Semantic proximity Read ↗

Familial exudative vitreoretinopathy: A report of an asymptomatic case with autosomal dominant inheritance detected using FZD4 molecular analysis.Semantic proximity Read ↗

Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy.Semantic proximity Read ↗

Identification of novel FZD4 mutations in Indian patients with familial exudative vitreoretinopathy.Semantic proximity Read ↗

Novel frizzled-4 gene mutations in chinese patients with familial exudative vitreoretinopathy.Semantic proximity Read ↗

The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease.Semantic proximity Read ↗

Severe form of familial exudative vitreoretinopathy caused by homozygous R417Q mutation in frizzled-4 gene.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: FZD4. Disease: familial exudative vitreoretinopathy.Semantic proximity Read ↗

Novel FZD4 and LRP5 mutations in a small cohort of patients with familial exudative vitreoretinopathy (FEVR).Semantic proximity Read ↗

Risk allele of the FZD4 gene for familial exudative vitreoretinopathy.Semantic proximity Read ↗

Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.Semantic proximity Read ↗

Mutation spectrum in a cohort with familial exudative vitreoretinopathy.Semantic proximity Read ↗

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