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

CRB1-associated retinal dystrophies in a Belgian cohort: genetic characteristics and long-term clinical follow-up.

The British journal of ophthalmology - 1 May 2022

Talib Mays, Van Cauwenbergh Caroline, De Zaeytijd Julie, Van Wynsberghe David, De Baere Elfride, Boon Camiel J F, Leroy Bart Peter

Abstract excerpt

AIM: To investigate the natural history in a Belgian cohort of CRB1-associated retinal dystrophies. METHODS: An in-depth retrospective study focusing on visual function and retinal structure. RESULTS: Forty patients from 35 families were included (ages: 2.5-80.1 years). In patients with a follow-up of >1 year (63%), the mean follow-up time was 12.0 years (range: 2.3-29.2 years). Based on the patient history,...

Read the complete abstract on PubMed

Topics

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

Share to Belgium
Share to Blindness

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electroretinography

Share to Eye Proteins

Share to Leber Congenital Amaurosis

Share to Macular Degeneration

Share to Retinal Dystrophies

Share to Retinitis Pigmentosa

Source

Identifiers

PMID: 33579689
DOI: 10.1136/bjophthalmol-2020-316781

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CRB1-associated retinal dystrophies in a Belgian cohort: genetic characteristics and long-term clinical follow-up.PMID 33579689Read ↗

CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History.Semantic proximity Read ↗

Genotypic and Phenotypic Characteristics of CRB1-Associated Retinal Dystrophies: A Long-Term Follow-up Study.Semantic proximity Read ↗

CRB1 mutations in inherited retinal dystrophies.Semantic proximity Read ↗

Clinical and mutational signatures of CRB1-associated retinopathies: a multicentre study.Semantic proximity Read ↗

A clinical and molecular characterisation of CRB1-associated maculopathy.Semantic proximity Read ↗

LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS: A Severe Phenotype With Considerable Interindividual Variability.Semantic proximity Read ↗

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.Semantic proximity Read ↗

CRB1 mutation spectrum in inherited retinal dystrophies.Semantic proximity Read ↗

A Novel Pathogenic Variant in CRB1 as the Cause of Non-Syndromic Retinitis Pigmentosa in a Geographical Isolate in Northern Italy.Semantic proximity Read ↗

CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 Isoforms.Semantic proximity Read ↗

Ophthalmological and Genetic Findings Associated with CRB1 Dysfunction in Autosomal Recessive Retinitis PigmentosaSemantic proximity Read ↗

Unveiling Inflammation-Like Retinal Remodeling in CRB1-Associated Inherited Retinal Dystrophies: Insights From a Multicenter Study.Semantic proximity Read ↗

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