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Enhanced S-Cone Syndrome 2
A retinal disease that is characterized by an increased number of cones in the retina, primarily those expressing S-cone opsins that is caused by compound heterozygous and homozygous mutation in the NRL gene on chromosom
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 retinal disease that is characterized by an increased number of cones in the retina, primarily those expressing S-cone opsins that is caused by compound heterozygous and homozygous mutation in the NRL gene on chromosom
Resources
Join the Enhanced S-Cone Syndrome 2 community
Talk with people who understand, share what helps, and find support from others living with enhanced s-cone syndrome 2. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.