Choroideremia
Choroideremia is a rare, inherited eye disorder characterized by:
- Progressive loss of the choroid, retina, and retinal pigment epithelium
- Night blindness
- Loss of peripheral vision
- Potential for central vision loss
Causes
- Genetic mutation: Mutations in the CHM gene
- X-linked inheritance: Primarily affects males
Symptoms
- Night blindness: Difficulty seeing in low light
- Peripheral vision loss: Loss of side vision
- Visual field defects: Blind spots or areas of decreased vision
Management
- Genetic counseling: Understanding inheritance patterns
- Low vision rehabilitation: Adapting to vision loss
- Research and clinical trials: Exploring potential treatments
- Regular eye exams: Monitoring disease progression
If you or a family member has choroideremia, consult with an eye care professional or genetic counselor for personalized guidance and support.
