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Autosomal Recessive Bestrophinopathy Presenting With a Macular Hole Retinal Detachment.

Authors :
Fouad YA
Tawfik CA
Nowara M
Source :
Journal of vitreoretinal diseases [J Vitreoretin Dis] 2022 Jul 20; Vol. 6 (4), pp. 312-315. Date of Electronic Publication: 2022 Jul 20 (Print Publication: 2022).
Publication Year :
2022

Abstract

Purpose: To report a case of autosomal recessive bestrophinopathy (ARB) that presented with macular hole retinal detachment (MHRD). Methods: A case report. Results: A 31-year-old male patient presented with rapid deterioration of vision in the left eye. On fundus examination, bilateral retinal deposits in both eyes, which were brightly hyperautofluorescent, and an MHRD in the left eye could be detected. An electrooculogram demonstrated absent light rise with abnormal Arden's ratio in both eyes. The patient was offered surgery for the MHRD but refused due to the guarded visual prognosis. Follow up of the patient after one year revealed progression of the retinal detachment. Genetic testing revealed a novel, homozygous missense mutation in the BEST1 gene, confirming the diagnosis of ARB. Conclusion: ARB can present with an MHRD. Counseling patients with inherited retinal dystrophies about the visual prognosis following surgical intervention is important.<br />Competing Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.<br /> (© The Author(s) 2022.)

Details

Language :
English
ISSN :
2474-1272
Volume :
6
Issue :
4
Database :
MEDLINE
Journal :
Journal of vitreoretinal diseases
Publication Type :
Report
Accession number :
37007926
Full Text :
https://doi.org/10.1177/24741264221098631