Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/j.jfo.2013.10.006 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Multimodal imaging findings of the fellow eye in Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis (SNIFR).
Retin Cases Brief Rep
January 2025
School of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Purpose: This study examines the multimodal imaging (MMI) findings in two cases of unilateral Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis (SNIFR), including detailed findings from the unaffected fellow eye.
Methods: Macular spectral domain optical coherence tomography (OCT) and 3x3 mm optical coherence tomography angiography (OCTA), microperimetry, full-field electroretinography (ff-ERG) for both the affected and the fellow eye were reviewed.
Results: The MMI findings were consistent across the two cases (71-year-old female and 60-year-old female).
Spontaneous Resolution and Asynchronous Onset of Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis in the Contralateral Eye.
J Vitreoretin Dis
December 2024
Retina Department, Fundación Hospital de Nuestra Señora de La Luz, Mexico City, Mexico.
Article Synopsis
- A 70-year-old woman was diagnosed with stellate nonhereditary idiopathic foveomacular retinoschisis, showing schisis cavities in the outer plexiform layer of her left eye through optical coherence tomography.
- No leakage was observed in fluorescein angiography, and other potential causes for her condition were ruled out.
- After five years, her visual acuity remained stable, the retinoschisis in her left eye resolved, but new cystoid spaces developed in the right eye, highlighting the need for multimodal imaging for monitoring such conditions.
Non-syndromic OTX2-associated pattern dystrophy: a 10-year multimodal imaging study.
Doc Ophthalmol
October 2024
Ocular Tissue Engineering Laboratory, Lions Eye Institute, Nedlands, WA, Australia.
Purpose: To report novel multimodal imaging features and long-term follow-up of Orthodenticle Homeobox 2 (OTX2)-associated pattern Gdystrophy.
Methods: A 14-year-old boy referred with glaucoma suspect and macular pigmentation underwent fundus autofluorescence imaging, optical coherence tomography, fluorescein and indocyanine green angiography, visual field test, microperimetry and electrophysiology over a ten-year period. Next-generation sequencing panel identified a de novo heterozygous likely pathogenic OTX2 variant, c.
Case report: A rare case of bilateral Leber's idiopathic stellate neuroretinitis.
Front Med (Lausanne)
March 2024
Department of Ophthalmology, Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, School of Clinical Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Background: Leber's idiopathic stellate neuroretinitis (LISN) is a rare disease characterized by disk edema, peripapillary and macular hard exudates, and often, the presence of vitreous cells. To enhance clinical understanding of the disease, a retrospective analysis was conducted on a patient diagnosed with LISN at our hospital, and discussions were held regarding its diagnosis and treatment.
Methods: We reviewed the medical records of a 26-year-old male patient whose main complaint was a decrease in visual acuity of both eyes for 4 days, which had worsened over the last day.
Stellate nonheritable idiopathic foveomacular retinoschisis in juveniles: case report.
BMC Ophthalmol
September 2023
Department of Ophthalmology, Hebei Medical University, Shijiazhuag, 050017, Hebei, China.
Background: Stellate nonhereditary idiopathic foveomacular retinoschisis (SNIFR) is a rare type of retinoschisis with a spoke-like splitting that occurs in the outer plexus layer. We present a case of stellate nonhereditary idiopathic foveomacular retinoschisis in a juvenile, in which two eyes show different development trends and macular retinoschisis could be associated with mechanical force in the Henle fibre layer. The removal of mechanical force can partially restore vision.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!