Community
Retinitis Pigmentosa 88
A retinitis pigmentosa characterized by night blindness and constriction of peripheral visual fields, with mildly reduced visual acuity that is caused by homozygous or compound heterozygous mutation in the RP1L1 gene on
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 retinitis pigmentosa characterized by night blindness and constriction of peripheral visual fields, with mildly reduced visual acuity that is caused by homozygous or compound heterozygous mutation in the RP1L1 gene on
Resources
Join the Retinitis Pigmentosa 88 community
Talk with people who understand, share what helps, and find support from others living with retinitis pigmentosa 88. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.