X-linked congenital stationary night blindness
Other Names for this Disease
- X-linked CSNB
- Congenital stationary night blindness with myopia
- Myopia-night blindness
- Congenital essential nyctalopia
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retina. People with this condition typically experience night blindness and other vision problems, including loss of sharpness (reduced visual acuity), severe nearsightedness (myopia), nystagmus, and strabismus. Color vision is typically not affected. These vision problems are usually evident at birth, but tend to be stable (stationary) over time. There are two major types of XLCSNB: the complete form and the incomplete form. Both types have very similar signs and symptoms. However, everyone with the complete form has night blindness, while not all people with the incomplete form have night blindness. The types are distinguished by their genetic cause.X-linked congenital stationary night blindness (XLCSNB) is a disorder of the
Last updated: 10/14/2011
- X-linked congenital stationary night blindness. Genetics Home Reference. May 2009; http://ghr.nlm.nih.gov/condition/x-linked-congenital-stationary-night-blindness. Accessed 10/14/2011.
- Genetics Home Reference (GHR) contains information on X-linked congenital stationary night blindness. This website is maintained by the National Library of Medicine.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss X-linked congenital stationary night blindness. Click on the link to view a sample search on this topic.