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Tuberous Sclerosis Complex

Tuberous sclerosis tuberous sclerosis complex.

Tuberous sclerosis complex. From wikipedia the free encyclopedia tuberous sclerosis complex 2 tsc2 also known as tuberin is a protein that in humans is encoded by the tsc2 gene. Help support we support individuals and families affected by tsc. Tsc is a genetic condition that can lead to growths in various organs of the body but those most commonly affected are the brain eyes heart kidney skin and lungs. Our dedicated advisers and active.

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. Tuberous sclerosis complex tsc involves abnormalities of the skin hypomelanotic macules confetti skin lesions facial angiofibromas shagreen patches fibrous cephalic plaques ungual fibromas. Tuberous sclerosis complex is a genetic disorder characterized by the growth of numerous noncancerous benign tumors in many parts of the body. International tuberous sclerosis complex research conference 2021.

Tuberous sclerosis two bur uhs skluh roh sis also called tuberous sclerosis complex is an uncommon genetic disorder that causes noncancerous benign tumors unexpected overgrowths of normal tissue to develop in many parts of the body.