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

Optical Coherence Tomography Examination of the Retinal Pigment Epithelium in Best Vitelliform Macular Dystrophy.

Ophthalmology - 1 Apr 2017

Qian Cynthia X, Charran Dionisio, Strong Cameron R, Steffens Timothy J, Jayasundera Thiran, Heckenlively John R

Abstract excerpt

PURPOSE: To describe the anatomic changes and natural history of vitelliform lesions in Best vitelliform macular dystrophy (BVMD) using spectral-domain optical coherence tomography (OCT). DESIGN: Prospective comparative case series. PARTICIPANTS: Twenty patients (40 eyes) with molecular confirmation of mutation in the BEST1 gene and 20 age-matched controls were included. METHODS: Color fundus photographs, fundus...

Read the complete abstract on PubMed

Topics

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

Share to Bestrophins
Share to Chloride Channels

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fluorescein Angiography

Share to Multimodal Imaging

Share to Optical Imaging

Share to Retinal Pigment Epithelium

Share to Tomography, Optical Coherence

Share to Vitelliform Macular Dystrophy

Source

Identifiers

PMID: 28187978
DOI: 10.1016/j.ophtha.2016.11.022

Genes

RPE
BEST1

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

Optical Coherence Tomography Examination of the Retinal Pigment Epithelium in Best Vitelliform Macular Dystrophy.PMID 28187978Read ↗

Clinical and molecular genetic analysis of best vitelliform macular dystrophy.Semantic proximity Read ↗

High-definition optical coherence tomography features in vitelliform macular dystrophy.Semantic proximity Read ↗

PHOTORECEPTOR INNER SEGMENT MORPHOLOGY IN BEST VITELLIFORM MACULAR DYSTROPHYSemantic proximity Read ↗

Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in Denmark.Semantic proximity Read ↗

Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 Mutations.Semantic proximity Read ↗

Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic Findings.Semantic proximity Read ↗

Functional and clinical data of Best vitelliform macular dystrophy patients with mutations in the BEST1 gene.Semantic proximity Read ↗

Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy.Semantic proximity Read ↗

Adult-Onset Foveomacular Vitelliform Dystrophy with a Novel BEST1 Variant: A Case Report and Multimodal Imaging CharacterizationSemantic proximity Read ↗

Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1.Semantic proximity Read ↗

The Spectrum of Subclinical Best Vitelliform Macular Dystrophy in Subjects with Mutations in<i>BEST1</i>GeneSemantic proximity Read ↗

Differential macular and peripheral expression of bestrophin in human eyes and its implication for best disease.Semantic proximity Read ↗

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