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Sveinsson Chorioretinal Atrophy
An eye disease characterized by presence in the fundus of progressive bilateral retinal and choroidal atrophy leading to central vision loss that is caused by heterozygous mutation in TEAD1 on 11p15.3.
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
An eye disease characterized by presence in the fundus of progressive bilateral retinal and choroidal atrophy leading to central vision loss that is caused by heterozygous mutation in TEAD1 on 11p15.3.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.