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

Oguchi disease masked by retinitis pigmentosa.

Documenta ophthalmologica. Advances in ophthalmology - 1 Oct 2011

Sonoyama Hiroko, Shinoda Kei, Ishigami Chie, Tada Yumi, Ideta Hidenao, Ideta Ryuichi, Takahashi Masayo, Miyake Yozo

Abstract excerpt

The purpose of this study was to report a patient with Oguchi disease whose ophthalmological characteristics were masked by retinitis pigmentosa (RP). The method used in this study was case report. A 53-year-old man had a progressive decrease in his visual acuity and was diagnosed with RP because of night blindness, fundoscopic findings, ring scotoma, and extinguished single-flash electroretinograms (ERGs)....

Read the complete abstract on PubMed

Topics

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

Share to Arrestin
Share to Dark Adaptation
Share to Eye Diseases, Hereditary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fluorescein Angiography

Share to Fundus Oculi

Share to Night Blindness

Share to Tomography, Optical Coherence

Share to Visual Fields

Source

Identifiers

PMID: 21922265
DOI: 10.1007/s10633-011-9286-x

Genes

SAG

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

Oguchi disease masked by retinitis pigmentosa.PMID 21922265Read ↗

Genetic analysis and clinical features of three Chinese patients with Oguchi disease.Semantic proximity Read ↗

Grk1 Missense Mutations in Type II Oguchi Disease: A Literature ReviewSemantic proximity Read ↗

Two novel compound heterozygous SAG mutations in an Italian patient with Oguchi disease: A genetic and multimodal retinal imaging study.Semantic proximity Read ↗

Wide-field true-colour imaging and clinical characterization of a novel GRK1 mutation in Oguchi disease.Semantic proximity Read ↗

Atypical presentation of Oguchi disease with severe cystoid macular edema and compound heterozygous SAG pathogenic variants.Semantic proximity Read ↗

A compound heterozygous mutation in the S-Antigen Visual Arrestin SAG gene in a Chinese patient with Oguchi type one: a case report.Semantic proximity Read ↗

Progression from Classical Oguchi Disease to Retinitis Pigmentosa after 50 Years.Semantic proximity Read ↗

Mutation analysis reveals novel and known mutations in SAG gene in first two Egyptian families with Oguchi disease.Semantic proximity Read ↗

A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease.Semantic proximity Read ↗

Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial LectureSemantic proximity Read ↗

Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.Semantic proximity Read ↗

Visual function and gene analysis in a family with Oguchi's disease.Semantic proximity Read ↗

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