Is tuberous sclerosis considered a genetic condition?

Tuberous sclerosis is indeed considered a genetic condition because it is caused by mutations in specific genes, primarily TSC1 and TSC2. These mutations lead to the development of benign tumors in various organs, including the brain, skin, kidneys, and heart. The condition exhibits an autosomal dominant inheritance pattern, meaning that it can be passed down from one affected parent to their children.

Moreover, the presence of these genetic mutations results in the characteristic manifestations of tuberous sclerosis, highlighting its basis in genetic factors rather than environmental influences. Thus, understanding that it is a genetic disorder is crucial for diagnosis, management, and counseling for affected individuals and their families.