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

High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy.

Ophthalmology - 1 Jan 2014

Kashani Amir H, Learned Daniel, Nudleman Eric, Drenser Kimberly A, Capone Antonio, Trese Michael T

Abstract excerpt

OBJECTIVE: To describe the prevalence and severity of familial exudative vitreoretinopathy (FEVR) in asymptomatic relatives of known symptomatic FEVR patients. DESIGN: Uncontrolled and retrospective case series at a single tertiary referral vitreoretinal practice. PARTICIPANTS: A total of 148 eyes of 74 subjects were studied. METHODS: A retrospective chart review was conducted of patients with a diagnosis of FEVR...

Read the complete abstract on PubMed

Topics

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

Share to Eye Diseases, Hereditary
Share to Familial Exudative Vitreoretinopathies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fluorescein Angiography

Share to Frizzled Receptors

Share to Gestational Age

Share to Retinal Diseases

Share to Retinal Vessels

Share to Tetraspanins

Source

Identifiers

PMID: 24084499
DOI: 10.1016/j.ophtha.2013.08.010

Genes

FZD4
NDP
TSPAN12

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy.PMID 24084499Read ↗

The spectrum of genetic mutations in patients with asymptomatic mild familial exudative vitreoretinopathy.Semantic proximity Read ↗

Genetic Characteristics and Clinical Manifestations of Foveal Hypoplasia in Familial Exudative Vitreoretinopathy.Semantic proximity Read ↗

Asymptomatic adults in a single family with familial exudative vitreoretinopathy and TSPAN12 variant.Semantic proximity Read ↗

Familial Exudative VitreoretinopathySemantic proximity Read ↗

Molecular Characterization of FZD4, LRP5, and TSPAN12 in Familial Exudative Vitreoretinopathy.Semantic proximity Read ↗

Reaching a FEVR Pitch: A Case Series of Familial Exudative Vitreoretinopathy in Northern Ireland.Semantic proximity Read ↗

Clinical and genetical features of probands and affected family members with familial exudative vitreoretinopathy in a large Chinese cohort.Semantic proximity Read ↗

Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy.Semantic proximity Read ↗

Familial exudative vitreoretinopathy and related retinopathies.Semantic proximity Read ↗

Unveiling novel LRP5 pathogenic variant in familial exudative vitreoretinopathy: Diverse phenotypic expressions in a mother-daughter duo.Semantic proximity Read ↗

The characteristics of digenic familial exudative vitreoretinopathy.Semantic proximity Read ↗

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

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