Gyrate atrophy with vitreous haemorrhage: a rare combination
A boy in his early adolescence presented with painless, progressive vision loss in both eyes over the past 4 months. Born of non-consanguineous parents with a normal delivery, he had no relevant family history. Physical examination revealed a thin build and an abnormal gait. Best-corrected visual
Authors
- Madhushmita Mahapatra
- Srikanta Kumar Padhy (ORCID: https://orcid.org/0000-0002-6453-5851)
- Sohini Mandal
- Divyansh Rughwani
Institutions
- L V Prasad Eye Institute (IN)
- Retina Institute (US)
Publication Details
- Journal
- BMJ Case Reports
- Published
- 2025-02-01
- DOI
- https://doi.org/10.1136/bcr-2024-262960
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00