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CURETINA personalized medicine in hereditary retinal degenerations

Type: Observational

Status of the trial: Completed

Orphan Drug Recognition: NA


  • Opening Date: 0000-00-00
  • Closing Date: 2018-06-30


Inclusion: Retinal degeneration caused by mutations in either of the genes CRB1, CRX, PROM1

Exclusion: Additional mutations in genes known for causing hereditary retinal degenerations; additional eye diseases influencing the retinal morphology and function (glaucoma, retinal detachment, etc.)

Children: Yes

Adults: Yes

Funder Type: national institution

HCP: Other investigators

Within ERN-EYE members

Principal investigators

Other investigators


  • Retinal Rare Eye Diseases (WG1)

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This ERN is supported by: