What is tuberous sclerosis?
Tuberous sclerosis is a rare genetic condition that causes mainly non-cancerous tumours to develop in different parts of the body such as the brain, skin, kidneys and lungs.
It can be present at birth but issues develop gradually.
What causes tuberous sclerosis?
Tuberous-sclerosis is caused by mutations in the TSC1 or TSC2 genes.
These genes are involved in regulating cell growth, and the mutations lead to uncontrolled growth and multiple tumours throughout the body.
It can happen spontaneously and isn’t inherited.
What are the symptoms of tuberous sclerosis?
Tuberous sclerosis symptoms can be either mild or severe and may include:
- Epilepsy
- Learning difficulties
- Skin abnormalities
- Breathing difficulties
- A build-up of fluid on the brain
There is no cure for tuberous sclerosis, but there are treatments that can help manage some of the symptoms.
If you’re concerned that you or your child may have tuberous sclerosis, it’s important to see a doctor for a diagnosis.