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Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness
Patients with the complete form of congenital stationary night blindness (CSNB) often have reduced visual acuity, myopia, impaired night vision, and sometimes nystagmus and strabismus, however, they seldom complain of color vision abnormality. A 17-year-old male who was at technical school showed ab...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743520/ https://www.ncbi.nlm.nih.gov/pubmed/23966763 http://dx.doi.org/10.2147/OPTH.S49496 |
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author | Tan, Xue Aoki, Aya Yanagi, Yasuo |
author_facet | Tan, Xue Aoki, Aya Yanagi, Yasuo |
author_sort | Tan, Xue |
collection | PubMed |
description | Patients with the complete form of congenital stationary night blindness (CSNB) often have reduced visual acuity, myopia, impaired night vision, and sometimes nystagmus and strabismus, however, they seldom complain of color vision abnormality. A 17-year-old male who was at technical school showed abnormalities in the color perception test for employment, and was referred to our hospital for a detailed examination. He had no family history of color vision deficiency and no other symptoms. During the initial examination, his best-corrected visual acuity was 1.2 in both eyes. His fundus showed no abnormalities except for somewhat yellowish reflex in the fovea of both eyes. Electroretinogram (ERG) showed a good response in cone ERG and 30 Hz flicker ERG, however, the bright flash, mixed rod and cone ERG showed a negative type with a reduced b-wave (positive deflection). There was no response in the rod ERG, either. From the findings of the typical ERG, the patient was diagnosed with complete congenital stationary night blindness. This case underscores the importance of ERG in order to diagnose the cause of a color vision anomaly. |
format | Online Article Text |
id | pubmed-3743520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37435202013-08-21 Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness Tan, Xue Aoki, Aya Yanagi, Yasuo Clin Ophthalmol Case Report Patients with the complete form of congenital stationary night blindness (CSNB) often have reduced visual acuity, myopia, impaired night vision, and sometimes nystagmus and strabismus, however, they seldom complain of color vision abnormality. A 17-year-old male who was at technical school showed abnormalities in the color perception test for employment, and was referred to our hospital for a detailed examination. He had no family history of color vision deficiency and no other symptoms. During the initial examination, his best-corrected visual acuity was 1.2 in both eyes. His fundus showed no abnormalities except for somewhat yellowish reflex in the fovea of both eyes. Electroretinogram (ERG) showed a good response in cone ERG and 30 Hz flicker ERG, however, the bright flash, mixed rod and cone ERG showed a negative type with a reduced b-wave (positive deflection). There was no response in the rod ERG, either. From the findings of the typical ERG, the patient was diagnosed with complete congenital stationary night blindness. This case underscores the importance of ERG in order to diagnose the cause of a color vision anomaly. Dove Medical Press 2013 2013-08-07 /pmc/articles/PMC3743520/ /pubmed/23966763 http://dx.doi.org/10.2147/OPTH.S49496 Text en © 2013 Tan et al. This work is published by Dove Medical Press Ltd, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License. The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Ltd, provided the work is properly attributed. |
spellingShingle | Case Report Tan, Xue Aoki, Aya Yanagi, Yasuo Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness |
title | Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness |
title_full | Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness |
title_fullStr | Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness |
title_full_unstemmed | Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness |
title_short | Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness |
title_sort | color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743520/ https://www.ncbi.nlm.nih.gov/pubmed/23966763 http://dx.doi.org/10.2147/OPTH.S49496 |
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