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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
General
sign/symptom
syndrome
retinal disease
Database Correlations
OMIM 608415
References
OMIM :accession 608415