Tuberous sclerosis (TS) is a neurocutaneous disorder, characterized by mental retardation, epilepsy, and facial angiofibromas. The incidence has been estimated to be 1 case per 6000 live births. Although rare, this disorder is a cause of mental retardation with severe epilepsy.1 Scientists have found manifestations of this disorder not only in brain and skin, but also in the eyes, heart, lungs, and kidneys, so it has been renamed tuberous sclerosis complex (TSC)
Tuberous sclerosis complex (TSC) is a rare genetic multisystem disease that involves brain, skin, ki...
Tuberous sclerosis complex (TSC) is a multisystem disorder, with significant renal cystic and solid ...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder with a birth incidence of...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder resulting in the growth o...
Tuberous sclerosis complex (TCS) is an autosomal dominant disease which comes under a group of disea...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Objective Tuberous sclerosis complex is an autosomal dominant neurocutaneous disease that presents w...
Tuberous sclerosis (TS) is a multiple-system disease involving the brain, skin, kidneys, heart and o...
textabstractTuberous Sclerosis Complex (TSC) is a multi-organ disorder, which is characterized by t...
Tuberous sclerosis complex (TSC) is a multisystem, autosomal dominant disorder affecting children an...
Tuberous sclerosis (TS) is a genetic disorder characterised by the triad of cutaneous lesions, epile...
Tuberous sclerosis complex (TSC) is known to cause severe intractable epilepsy and mental retardatio...
Tuberous sclerosis (also known as tuberous sclerosis complex [TSC]) is a multisystem genetic disorde...
Tuberous sclerosis (TS) otozomal dominant geçişli, birçok organ sisteminde hamartomlarla karakterize...
Tuberous sclerosis complex (TSC) is a rare genetic multisystem disease that involves brain, skin, ki...
Tuberous sclerosis complex (TSC) is a multisystem disorder, with significant renal cystic and solid ...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder with a birth incidence of...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder resulting in the growth o...
Tuberous sclerosis complex (TCS) is an autosomal dominant disease which comes under a group of disea...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Objective Tuberous sclerosis complex is an autosomal dominant neurocutaneous disease that presents w...
Tuberous sclerosis (TS) is a multiple-system disease involving the brain, skin, kidneys, heart and o...
textabstractTuberous Sclerosis Complex (TSC) is a multi-organ disorder, which is characterized by t...
Tuberous sclerosis complex (TSC) is a multisystem, autosomal dominant disorder affecting children an...
Tuberous sclerosis (TS) is a genetic disorder characterised by the triad of cutaneous lesions, epile...
Tuberous sclerosis complex (TSC) is known to cause severe intractable epilepsy and mental retardatio...
Tuberous sclerosis (also known as tuberous sclerosis complex [TSC]) is a multisystem genetic disorde...
Tuberous sclerosis (TS) otozomal dominant geçişli, birçok organ sisteminde hamartomlarla karakterize...
Tuberous sclerosis complex (TSC) is a rare genetic multisystem disease that involves brain, skin, ki...
Tuberous sclerosis complex (TSC) is a multisystem disorder, with significant renal cystic and solid ...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder with a birth incidence of...