Browser update


Clinical Cases
Age range -
Instants range -
Exam type

Congenital Stationary Night Blindness

Congenital Stationary Night Blindness - Start  
Congenital Stationary Night Blindness - End  

Oguchi disease is an autosomal recessive retinal disorder characterized by congenital stationary night blindness and the Mizuo-Nakamura phenomenon, since young childhood or birth with normal day vision.

The retina has a typical diffuse golden-yellow or silver-gray discoloration of the fundus in the presence of light that disappears after dark-adaptation and appears again after the onset of light. This phenomenon is thought to be caused by the overstimulation of rod cells.

No evidence of spicules, macular changes or chorioretinal atrophy is observed. The visual acuity and the caliber of retinal blood vessels are normal and the cone response on electroretinogram is normal.

The diagnosis based on fundoscopy and electroretinography is confirmed by genetic tests.

Differential Diagnosis

  • X-linked retinitis pigmentosa
  • Early onset cone rod dystrophy
  • Progressive cone dystrophy
Clinical Cases 8 0