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.
CITATION STYLE
Tsang, S. H., & Sharma, T. (2018). Congenital stationary night blindness. In Advances in Experimental Medicine and Biology (Vol. 1085, pp. 61–64). Springer New York LLC. https://doi.org/10.1007/978-3-319-95046-4_13
Mendeley helps you to discover research relevant for your work.