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Tuberous Sclerosis 2
A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and is caused by autosomal dominant inheritance of heterozygous mutation in the TSC2 gene, which encodes tuberin, on chromosome 16p13.
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 tuberous sclerosis that is characterized by hamartomas in multiple organ systems and is caused by autosomal dominant inheritance of heterozygous mutation in the TSC2 gene, which encodes tuberin, on chromosome 16p13.
Resources
Join the Tuberous Sclerosis 2 community
Talk with people who understand, share what helps, and find support from others living with tuberous sclerosis 2. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.