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DOI: 10.1055/a-2776-4568
Are There Night Driving Restrictions for Patients with Incomplete Congenital Stationary Night Blindness?
Nächtliches Fahrverbot für Patienten mit inkompletter kongenitaler stationärer Nachtblindheit?Autor*innen
Background
Congenital stationary night blindness refers to a heterogeneous group of rare, inherited retinal disorders characterized by congenital, non-progressive visual impairment [1], [2]. Among the different subtypes of CSNB, the incomplete form is associated with an altered signal transmission from the photoreceptors to both ON- and OFF-bipolar cells, impairing visual processing [3]. Clinically, patients with incomplete CSNB present with nyctalopia, reduced visual acuity, and photophobia [4]. These symptoms can significantly affect daily functioning, particularly tasks that require adequate vision under low-light conditions.
In Switzerland, the Traffic Licensing Ordinance (TLO) defines medical criteria for assessing driving fitness [5], [6]. These include specific thresholds for visual acuity, visual field, and functional vision under mesopic conditions, with optional assessments of contrast sensitivity and glare sensitivity when relevant. Individuals with significant impairments in these domains may face restrictions, particularly regarding nighttime driving. Given the visual limitations associated with incomplete CSNB, it is essential to assess whether affected individuals should be restricted from driving at night to ensure both personal and public safety.
Publikationsverlauf
Eingereicht: 24. September 2025
Angenommen: 18. Dezember 2025
Artikel online veröffentlicht:
17. Februar 2026
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References
- 1 Schubert G, Bornschein H. Beitrag zur Analyse des menschlichen Elektroretinogramms. Ophthalmologica 1952; 123: 396-413
- 2 Miyake Y, Yagasaki K, Horiguchi M. et al. Congenital stationary night blindness with negative electroretinogram. A new classification. Arch Ophthalmol 1986; 104: 1013-1020
- 3 Zeitz C, Robson AG, Audo I. Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms. Prog Retin Eye Res 2015; 45: 58-110
- 4 Bijveld MM, Florijn RJ, Bergen AA. et al. Genotype and phenotype of 101 Dutch patients with congenital stationary night blindness. Ophthalmology 2013; 120: 2072-2081
- 5 Blaser F, Schneebeli M, Keller KH. et al. National Consensus on the Assessment of Visual Function for Driving in Switzerland. Klin Monbl Augenheilkd 2025; 242: 507-514
- 6 Schweizerische Eidgenossenschaft. Strassenverkehrsgesetz (SVG). Accessed 30.06.2025 at: https://www.fedlex.admin.ch/eli/cc/1959/679_705_685/de
- 7 Bech-Hansen NT, Naylor MJ, Maybaum TA. et al. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Nat Genet 1998; 19: 264-267
- 8 William A, Kohl S, Zeitz C. et al. Macular sensitivity in patients with congenital stationary night-blindness. Br J Ophthalmol 2019; 103: 1507-1510
- 9 Yu M, Hao W, Wang M. et al. Characterizing Retinal Sensitivity and Structure in Congenital Stationary Night Blindness: A Combined Microperimetry and OCT Study. Invest Ophthalmol Vis Sci 2024; 65: 35
