Pigmented paravenous retinochoroidal atrophy and retinitis pigmentosa-like phenotype in the same patient: A case series
PPRCA was demonstrated to be a non-progressive or slowly progressive disease, instead the eye with RP-like phenotype showed a progressive visual impairment, highlighting the importance of shedding light on this condition. Its etiology remains unclear: a genetic trait with different phenotype between the two eyes is conceivable, as well as a potential role of ARAs.
Authors
- Leonardo Colombo (ORCID: https://orcid.org/0000-0002-9556-994X)
- G Bonetti (ORCID: https://orcid.org/0000-0002-0666-9616)
- Matteo Bertelli (ORCID: https://orcid.org/0000-0002-7646-2872)
- Luca Rossetti (ORCID: https://orcid.org/0000-0002-7027-3173)
- Paolo Enrico Maltese (ORCID: https://orcid.org/0000-0002-1974-4937)
- Salvatore Martella (ORCID: https://orcid.org/0009-0005-8336-1833)
- Roberta Rissotto
- Simona Romano (ORCID: https://orcid.org/0000-0002-9401-5814)
Institutions
- University of Milan (IT)
- MultiMedica (IT)
- Ospedale San Paolo (IT)
- Center for Neuroscience and Cognitive Systems (IT)
Publication Details
- Journal
- European Journal of Ophthalmology
- Published
- 2024-08-16
- DOI
- https://doi.org/10.1177/11206721241275730
- Primary Topic
- Retinal Development and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00