Skip to main content

Congenital Stationary Night Blindness

  • Chapter
  • First Online:
Atlas of Inherited Retinal Diseases

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 1085))

Abstract

In congenital stationary night blindness (CSNB), there is a defect in rod photoreceptor signal transmission. This disorder of night vision is non-progressive. The most common inheritance pattern is X-linked, though autosomal recessive and autosomal dominant patterns have been described (Fig. 13.1). There is genetic heterogeneity within these types.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 189.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 249.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Suggested Reading

  • Marmor MF. Long-term follow-up of the physiologic abnormalities and fundus changes in fundus albipunctatus. Ophthalmology. 1990;97:380–4.

    Article  CAS  Google Scholar 

  • Sergouniotis PI, Sohn EH, Li Z, McBain VA, Wright GA, Moore AT, et al. Phenotypic variability in RDH5 retinopathy (Fundus Albipunctatus). Ophthalmology. 2011;118:1661–70.

    Article  Google Scholar 

  • Usui T, Tanimoto N, Ueki S, Takagi M, Hasegawa S, Abe H, et al. ERG rod a-wave in Oguchi disease. Vision Res. 2004;44:535–40.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tarun Sharma .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2018 Springer International Publishing AG, part of Springer Nature

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Tsang, S.H., Sharma, T. (2018). Congenital Stationary Night Blindness. In: Tsang, S., Sharma, T. (eds) Atlas of Inherited Retinal Diseases. Advances in Experimental Medicine and Biology, vol 1085. Springer, Cham. https://doi.org/10.1007/978-3-319-95046-4_13

Download citation

Publish with us

Policies and ethics