Definition: a progressive retinal degeneration characterized by bilateral nyctalopia, constricted visual fields, electroretinogram abnormalities, and pigmentary infiltration of the inner retinal layers; may be sporadic or demonstrate autosomal dominant [MIM*180100], autosomal recessive, or X-linked inheritance [MIM*268000, *312600, *312610].
Synonym(s): pigmentary retinopathy
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