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X-Linked Juvenile Retinoschisis 1
A retinoschisis characterized by schisis (splitting) of the neural retina leading to reduced visual acuity in males due that is caused by the RS1 gene on chromosome Xp22.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
A retinoschisis characterized by schisis (splitting) of the neural retina leading to reduced visual acuity in males due that is caused by the RS1 gene on chromosome Xp22.
Resources
Join the X-Linked Juvenile Retinoschisis 1 community
Talk with people who understand, share what helps, and find support from others living with x-linked juvenile retinoschisis 1. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.