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

Foveal Hypoplasia in Patients with Stickler Syndrome.

Ophthalmology - 1 Jun 2017

Matsushita Itsuka, Nagata Tatsuo, Hayashi Takaaki, Kimoto Kenichi, Kubota Toshiaki, Ohji Masahito, Kusaka Shunji, Kondo Hiroyuki

Abstract excerpt

PURPOSE: To determine the microstructure of the fovea in patients with Stickler syndrome using imaging by spectral-domain optical coherence tomography (SD OCT) and swept-source OCT. DESIGN: Retrospective case series study. PARTICIPANTS: A total of 39 eyes of 25 patients with genetically confirmed Stickler syndrome were studied. METHODS: All of the patients had mutations in the COL2A1 gene and were diagnosed with...

Read the complete abstract on PubMed

Topics

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

Share to Retinal Detachment
Share to Fluorescein Angiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fovea Centralis

Share to Arthritis

Share to Collagen Type II

Share to Connective Tissue Diseases

Share to Eye Abnormalities

Share to Tomography, Optical Coherence

Source

Identifiers

PMID: 28283280
DOI: 10.1016/j.ophtha.2017.01.046

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Foveal Hypoplasia in Patients with Stickler Syndrome.PMID 28283280Read ↗

Phenotypic Spectrum of the Foveal Configuration and Foveal Avascular Zone in Patients With Alport Syndrome.Semantic proximity Read ↗

Peripapillary Hyperreflective Ovoid Mass-Like Structures in Stickler Syndrome.Semantic proximity Read ↗

Clinical and molecular genetics of Stickler syndromeSemantic proximity Read ↗

Stickler syndrome: an underdiagnosed disease. Report of a family.Semantic proximity Read ↗

Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene.Semantic proximity Read ↗

Radial perivascular retinal degeneration: a key to the clinical diagnosis of an ocular variant of Stickler syndrome with minimal or no systemic manifestations.Semantic proximity Read ↗

Stickler syndrome, ocular-only variants and a key diagnostic role for the ophthalmologist.Semantic proximity Read ↗

Stickler syndrome: correlation between vitreoretinal phenotypes and linkage to COL 2A1.Semantic proximity Read ↗

Clinical Insights Into Foveal Morphology in Albinism.Semantic proximity Read ↗

Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1.Semantic proximity Read ↗

Ocular complications and prophylactic strategies in Stickler syndrome: a systematic literature review.Semantic proximity Read ↗

Genetic variant of Stickler's syndrome.Semantic proximity Read ↗

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