X-linked retinoschisis
ORPHA:792· ICD-10 Q14.1
Definition
A rare disorder involving multiple structure of the eye characterized by reduced visual acuity in males due to juvenile macular degeneration. Clinical features such as vitreous hemorrhage, retinal detachment, and neovascular glaucoma can be observed in advanced stages.
- Prevalence
- 1-9 / 100 000
- Inheritance
- X-linked recessive
- Age of onset
- Adolescent, Adult, Childhood, Infancy