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GTR Home > Conditions/Phenotypes > Prolonged electroretinal response suppression 2

Summary

Prolonged electroretinal response suppression-2 (PERRS2), also referred to as bradyopsia-2, is an autosomal recessive childhood-onset retinopathy characterized by markedly delayed dark and light adaptation, mild photophobia, difficulty seeing moving objects, moderately reduced visual acuity, normal color vision, normal fundi, and reduced rod and cone responses with prolonged recovery on electrophysiologic assessment (summary by Michaelides et al., 2010). For a discussion of genetic heterogeneity of prolonged electroretinal response suppression (PERRS), see 608415. [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: PERRS, PERRS2, R9AP, RGS9, RGS9BP
    Summary: regulator of G protein signaling 9 binding protein

Clinical features

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