prolonged electroretinal response suppression (PERRS); bradyopsia

Genetics

• associated with defects in RGS9 or RGS9BP genes

Clinical manifestations

• difficulty adjusting to sudden changes in luminance levels mediated by cones

More general terms

• sign/symptom
• syndrome
• retinal disease

Database

• OMIM: https://mirror.omim.org/entry/608415