MULTIMODAL IMAGING FINDINGS OF THE FELLOW EYE IN STELLATE NONHEREDITARY IDIOPATHIC FOVEOMACULAR RETINOSCHISIS
Although stellate nonhereditary idiopathic foveomacular retinoschisis typically presents as a unilateral condition, our findings suggest that patients may have an inherent structural predisposition to macular schisis, resulting in subtle functional impairments. We hypothesize that the structural damage may involve the macular Muller cells. These observations highlight the importance of further studies to understand stellate nonhereditary idiopathic foveomacular retinoschisis's pathophysiology and inform therapeutic approaches.
Authors
- Alessandro Arrigo (ORCID: https://orcid.org/0000-0003-4715-8414)
- Angela Malegori
- Alessio Antropoli (ORCID: https://orcid.org/0000-0001-9630-0830)
- Maurízio Battaglia Parodi (ORCID: https://orcid.org/0000-0002-0385-7961)
- Maria Vittoria Cicinelli (ORCID: https://orcid.org/0000-0003-2938-0409)
- Francesco Bandello (ORCID: https://orcid.org/0000-0003-3238-9682)
- Lorenzo Bianco (ORCID: https://orcid.org/0000-0002-4023-5387)
- Luigi Bruno (ORCID: https://orcid.org/0000-0002-6745-0466)
- Sebastiano Del Fabbro
- Soufiane Bousyf
Institutions
- Vita-Salute San Raffaele University (IT)
- Istituti di Ricovero e Cura a Carattere Scientifico (IT)
- Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele (IT)
Publication Details
- Journal
- Retinal Cases & Brief Reports
- Published
- 2025-01-16
- DOI
- https://doi.org/10.1097/icb.0000000000001718
- Citations
- 1
- Primary Topic
- Ocular Diseases and Behçet’s Syndrome
- Type
- article
- Field-Weighted Citation Impact
- 1.71