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Electrophysiological characteristics and gene analysis of children with congenital stationary night blindness without fundus abnormalities
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Dongmei QI, Shujia HUO, Xu ZHOU, Tao YU
Journal of Army Medical University | 2025, 47(20) : 2540 - 2547
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Journal of Army Medical University | 2025, 47(20): 2540-2547
• Clinical Medicine •
Electrophysiological characteristics and gene analysis of children with congenital stationary night blindness without fundus abnormalities
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Dongmei QI, Shujia HUO, Xu ZHOU, Tao YU
Affiliations
  • 1Department of Ophthalmology,First Affiliated Hospital/Southwest Hospital,Army Medical University (Third Military Medical University),Chongqing,China
Published: 2025-10-30 doi: 10.16016/j.2097-0927.202507102
Outline
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Objective

To analyze the electrophysiological and genetic examination results of children with congenital stationary night blindness (CSNB) without fundus abnormalities.

Methods

A retrospective study was conducted on 11 children diagnosed with CSNB in our department from August 2019 to March 2025. Their full-field electroretinogram (ffERG) and the results of genetic testing were analyzed.

Results

Among the 11 patients, there were 10 males and 1 female, at a mean age of 7.5±2.1 years. In the optometry, 1 patient had hyperopia and the other had myopia, and all of them obtained a corrected visual acuity of 0.48±0.11 after wearing glasses. In fundus photography examination, except for the leopard pattern changes in high myopia, no obvious abnormalities were found in the remaining fundus. In ffERG examination for all patients, the amplitude of the a-wave of scotopic ERG 3.0/10.0 was normal or slightly to moderately decreased, the amplitude of the b-wave was decreased significantly, and the amplitude ratio of the b-wave to the a-wave was <1, showing a negative-phase wave, which belonged to the CSNB Schubert-Bornschein waveform. The results of genetic test revealed that all the 11 patients carried pathogenic mutations, including 6 cases with CACNA1F mutations, 2 cases with GPR179 mutations, 2 cases with NYX mutations, and 1 case with GRM6 mutation.

Conclusion

For children with normal fundus manifestations but corrected visual acuity lower than normal after wearing glasses, ffERG examination should be carried out as soon as possible to screen for CSNB, and a diagnosis should be made in combination with genetic testing. This is helpful for evaluating the heredity and prognosis of the disease, increasing the chance of early detection, and reducing excessive amblyopia training and treatment.

children  /  congenital stationary night blindness  /  fundus photography  /  electroretinogram  /  genetic testing
齐冬梅, 霍姝佳, 周序, 余涛. 正常眼底型先天性静止性夜盲患儿的电生理特征与基因分析. 陆军军医大学学报, 2025 , 47 (20) : 2540 -2547 . DOI: 10.16016/j.2097-0927.202507102
Dongmei QI, Shujia HUO, Xu ZHOU, Tao YU. Electrophysiological characteristics and gene analysis of children with congenital stationary night blindness without fundus abnormalities[J]. Journal of Army Medical University, 2025 , 47 (20) : 2540 -2547 . DOI: 10.16016/j.2097-0927.202507102
Year 2025 volume 47 Issue 20
14
3
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Article Info
doi: 10.16016/j.2097-0927.202507102
  • Receive Date:2025-07-29
  • Online Date:2026-10-30
  • Published:2025-10-30
Article Data
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History
  • Received:2025-07-29
  • Revised:2025-10-17
Affiliations
    1Department of Ophthalmology,First Affiliated Hospital/Southwest Hospital,Army Medical University (Third Military Medical University),Chongqing,China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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