Tuberous sclerosis complex (TSC) is a relatively rare autosomal dominant neurocutaneous
disorder secondary to mutations in the TSC1 or TSC2 tumor suppressor genes. Although …

Tuberous sclerosis complex (TSC) is an autosomal-dominant neurocutaneous disease with
high phenotypic variability. The incidence is approximately one in 5000–10,000 births. TSC …

Tuberous sclerosis complex (TSC) is a genetically determined hamartomatous
neurocutaneous disease with high phenotypic variability. TSC is characterized by …

Objective To study the clinical features and identify unique renal neoplasia subtypes and
their prognostic implications in individuals with tuberous sclerosis complex (TSC). Patients …

Tuberous sclerosis complex (TSC) is a neurocutaneous autosomaldominant genetic
syndrome marked by development of hamartomatous lesions arising from dysfunction of the …

Tuberous sclerosis complex (TSC) is a neurocutaneous syndrome that can affect the brain,
skin, eyes, kidneys, heart, and lungs. TSC alters cellular proliferation and differentiation …

Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem neurocutaneous
disorder. TSC results in hamartomatous lesions primarily involving the skin, central nervous …

Introduction Tuberous sclerosis complex (TSC) is a rare autosomal dominant disorder
affecting multiple systems, due to inactivating mutations of TSC1 or TSC2 mTOR pathway …

Tuberous sclerosis complex (TSC) is an autosomal-dominant neurocutaneous disorder with
a high spontaneous mutation rate. Understanding of this disorder has greatly increased in …

Tuberous sclerosis complex (TSC) is a genetically inherited neurocutaneous disorder that
may affect many organ systems, including brain, skin, eyes, heart, lungs, liver, and kidneys …