Unilateral retinitis pigmentosa in Von Recklinghausen disease: A rare occurrence
Retinitis pigmentosa (RP) is hereditary progressive retinal dystrophy causing symmetrical affliction of both eyes. Neurofibromatosis 1 (NF1)/Von Recklinghausen disease is a hereditary neurocutaneous disorder with ocular involvement. But, occurrence of retinitis pigmentosa in NF1 is very uncommon, and unilateral RP in this scenario is a rare occurrence. This case report is of a male patient with NF1 presenting with unilateral RP on ophthalmological examination. This case is being presented for its rarity.
Authors
- Kavin Bhogar
- Taru Dewan (ORCID: https://orcid.org/0000-0001-9529-9313)
- Isha Tyagi (ORCID: https://orcid.org/0000-0002-0045-127X)
- Kumari Ritu
Institutions
- Atal Bihari Vajpayee Institute of Medical Sciences and Dr. Ram Manohar Lohia Hospital (IN)
- All India Institute of Medical Sciences, Deoghar (IN)
- Institute of Medical Sciences (IN)
Publication Details
- Journal
- Indian Journal of Ophthalmology - Case Reports
- Published
- 2024-10-01
- DOI
- https://doi.org/10.4103/ijo.ijo_911_24
- Primary Topic
- Retinal Development and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00