retinitis pigmentosa type 1 (RP1)

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Introduction

see retinitis pigmentosa

Pathology

Genetics

  • associated with defects in RP1 (ORP1)

Clinical manifestations

  • night vision blindness
  • loss of midperipheral visual field.
  • as the condition progresses, peripheral field vision is lost & eventually central vision as well

More general terms

References

Database