dominant pericentral pigmentary retinopathy
MeSH: C566713ORPHA: 791
Overview
retinitis pigmentosa that is characterized pigmentary retinal degeneration with onset in the teens leading to blindness in the sixth ans seventh decades of life
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with dominant pericentral pigmentary retinopathy, sourced from HPO and Orphanet clinical annotations.
Conductive hearing impairmentSensorineural hearing impairmentVisual impairmentAbnormal electroretinogramRetinal degenerationPhotophobiaBlindnessNystagmusOptic atrophyProgressive night blindnessAbnormal retinal pigmentationSpicular pigmentation of the retinaAbnormal retinal vascular morphologyGlaucomaOptic disc pallorKeratoconusOphthalmoplegiaNyctalopiaHyperinsulinemiaRetinal atrophyPosterior subcapsular cataractAttenuation of retinal blood vesselsPeripheral visual field lossCystoid macular edemaOptic disc drusenAbnormal full-field electroretinogramAbnormal central response of multifocal electroretinogramPhotoreceptor outer segment loss on macular OCTColor vision defectReduced visual acuityPhotopsia
Classification & Codes
MeSH Code
C566713Orphanet Code
ORPHA:791dominant pericentral pigmentary retinopathy
| MeSH | C566713 |
| Orphanet | ORPHA:791 |
| Treatments | 0 drug(s) |
| Symptoms on record | 31 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO