All of the following are seen in Favre-Goldmann syndrome except?
A. Ectopia lentis
D. Pigmentary changes similar to retinitis pigmentosa
Correct answer : A. Ectopia lentis
- Favre-Goldmann syndrome is an autosomal recessive condition.
- It usually presents in childhood with nyctalopia.
- Central and peripheral retinoschisis is present.
- There is marked pigmentary changes similar to retinitis pigmentosa.
Ref: Comprehensive Ophthalmology, A. K. Khurana, 4th edition, p271.