Three cases of acute-onset bilateral photophobia.
Acute Disease
Adult
Aged
Diagnosis, Differential
Electroretinography
/ methods
Eye Diseases, Hereditary
/ complications
Female
Fluorescein Angiography
Follow-Up Studies
Fundus Oculi
Genetic Diseases, X-Linked
/ complications
Humans
Myopia
/ complications
Night Blindness
/ complications
Photophobia
/ diagnosis
Retrospective Studies
Tomography, Optical Coherence
Visual Acuity
Acquired retinal disease
Incomplete-type congenital stationary night blindness
Negative-type ERG
Post-phototransduction abnormality
Journal
Japanese journal of ophthalmology
ISSN: 1613-2246
Titre abrégé: Jpn J Ophthalmol
Pays: Japan
ID NLM: 0044652
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
received:
10
08
2018
accepted:
15
11
2018
pubmed:
4
1
2019
medline:
28
3
2019
entrez:
4
1
2019
Statut:
ppublish
Résumé
To report the findings in 3 cases of bilateral negative electroretinograms (ERGs) with acute onset of photophobia. Retrospective case series. The medical charts of the 3 patients were reviewed. A 43-year-old woman, a 68-year-old woman, and a 41-year-old woman were referred to Nagoya University Hospital. Their main symptom was bilateral acute photophobia. None of the patients had any systemic diseases or specific medical history. The decimal best-corrected visual acuity (> 0.8) and Humphrey visual fields (mean deviation > -3 dB) were relatively well preserved in all 3 patients. The optical coherence tomography (OCT) and fundus autofluorescence findings were essentially normal. Fluorescein angiography showed mild leakage in 1 patient but no abnormality in the other 2 patients. However, the ERGs of the 3 patients had the features of abnormal ERGs found in patients with incomplete congenital stationary night blindness (CSNB). Exome analyses found no pathogenic variants related to known CSNB-related genes. The symptoms and ERGs of the 3 patients have not progressed or recovered after a relatively long follow-up period. The ERG characteristics of 3 patients with bilateral photophobia were similar to those of incomplete CSNB, suggesting post-phototransductional abnormalities. The symptoms and genetic analyses indicated the possibility of an acquired condition rather than a hereditary retinal disease.
Identifiants
pubmed: 30604114
doi: 10.1007/s10384-018-00649-0
pii: 10.1007/s10384-018-00649-0
doi:
Types de publication
Case Reports
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
172-180Subventions
Organisme : Japan Society for the Promotion of Science
ID : 16K11320
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