Oguchi disease

Oguchi disease
Other namesCongenital stationary night blindness, Oguchi type 1 or Oguchi disease 1[1]
Oguchi disease has an autosomal recessive pattern of inheritance.
SpecialtyNeurology Edit this on Wikidata

Oguchi disease is an autosomal recessive[2] form of congenital stationary night blindness associated with fundus discoloration and abnormally slow dark adaptation.

  1. ^ Cite error: The named reference omim was invoked but never defined (see the help page).
  2. ^ Maw, M. A.; John, S.; Jablonka, S.; Müller, B.; Kumaramanickavel, G.; Oehlmann, R.; Denton, M. J.; Gal, A. (May 1995). "Oguchi disease: suggestion of linkage to markers on chromosome 2q". Journal of Medical Genetics. 32 (5): 396–398. doi:10.1136/jmg.32.5.396. PMC 1050438. PMID 7616550.