Three cases of acute-onset bilateral photophobia.


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
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

172-180

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 16K11320

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Auteurs

Shinji Ueno (S)

Department of Ophthalmology, Nagoya University Graduate School of Medicine, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550, Japan. ueno@med.nagoya-u.ac.jp.

Daiki Inooka (D)

Department of Ophthalmology, Nagoya University Graduate School of Medicine, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550, Japan.

Monika Meinert (M)

Department of Ophthalmology, Nagoya University Graduate School of Medicine, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550, Japan.
Department of Ophthalmology, Lund University, Lund, Sweden.

Yasuki Ito (Y)

Department of Ophthalmology, Nagoya University Graduate School of Medicine, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550, Japan.

Kazushige Tsunoda (K)

National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.

Kaoru Fujinami (K)

National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Department of Genetics, UCL Institute of Ophthalmology, London, UK.

Takeshi Iwata (T)

National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.

Hisao Ohde (H)

Department of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.

Hiroko Terasaki (H)

Department of Ophthalmology, Nagoya University Graduate School of Medicine, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550, Japan.

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Classifications MeSH