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tuberous sclerosis - traduction vers arabe
![TSC is inherited in an [[autosomal dominant]] fashion.](https://commons.wikimedia.org/wiki/Special:FilePath/Autosomal dominant - en.svg?width=200 "TSC is inherited in an [[autosomal dominant]] fashion.")
![[[Désiré-Magloire Bourneville]]](https://commons.wikimedia.org/wiki/Special:FilePath/Désiré-Magloire Bourneville.jpg?width=200 "[[Désiré-Magloire Bourneville]]")
Wikipédia
Tuberous sclerosis complex (TSC) is a rare multisystem autosomal dominant genetic disease that causes non-cancerous tumours to grow in the brain and on other vital organs such as the kidneys, heart, liver, eyes, lungs and skin. A combination of symptoms may include seizures, intellectual disability, developmental delay, behavioral problems, skin abnormalities, lung disease, and kidney disease.
TSC is caused by a mutation of either of two genes, TSC1 and TSC2, which code for the proteins hamartin and tuberin, respectively, with TSC2 mutations accounting for the majority and tending to cause more severe symptoms. These proteins act as tumor growth suppressors, agents that regulate cell proliferation and differentiation.
Prognosis is highly variable and depends on the symptoms, but life expectancy is normal for many.
The prevalence of the disease is estimated to be 7 to 12 in 100,000. The disease is often abbreviated to tuberous sclerosis, which refers to the hard swellings in the brains of patients, first described by French neurologist Désiré-Magloire Bourneville in 1880.
