Tuberous sclerosis is a disease characterised by convulsive seizures, mental deficiency and angiofibromas. These angiofibromas are hamartomas consisting of hyperplastic connective and vascular tissue. A case is reported where multiple angiofibromas of the face resulted in significant disfigurement. The lesions were treated by shaving and dermabrasion; the short-term result was very satisfactory.S Afr Med J 1989; 76: 169-17
Clinical manifestations of tuberous sclerosis (TS) are variable, and oral involvement occurs in less...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Introduction: Tuberous sclerosis complex (TSC) is a neurocutaneous syndrome produced by a number of ...
Tuberous sclerosis can manifest itself by multiple facial nodules affecting primarily the nose, chee...
Tuberous sclerosis or tuberous sclerosis complex (TSC) is an autosomal dominant inherited disease ch...
Tuberous sclerosis complex is an autosomal dominant disorder that can cause nonmalignant hamartomas ...
Tuberous Sclerosis Complex (TSC) is a multisystem genetic disease characterized by cutaneous and ext...
ABSTRACT: Tuberous sclerosis complex is a type of genetic multisystem disease that causes hamartomas...
Introduction: Tuberous sclerosis complex (TSC) is a rare, genetic disease that leads to neurological...
Tuberous sclerosis is a rare congenital disorder with an incidence of 1 in 6000 births. The classic ...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder resulting in the growth o...
Tuberous Sclerosis Complex is an autosomal dominant phakomatosis. This neurocutaneous disorder usual...
Tuberous sclerosis complex (TSC) is an inherited neurocutaneous disorder with multisystem involvemen...
Tuberous sclerosis complex is a genetic disease characterized by multisystemic hamartomas with varia...
Tuberous sclerosis is a rare autosomal dominant disorder. Myofibroblasts are cells with a hybrid phe...
Clinical manifestations of tuberous sclerosis (TS) are variable, and oral involvement occurs in less...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Introduction: Tuberous sclerosis complex (TSC) is a neurocutaneous syndrome produced by a number of ...
Tuberous sclerosis can manifest itself by multiple facial nodules affecting primarily the nose, chee...
Tuberous sclerosis or tuberous sclerosis complex (TSC) is an autosomal dominant inherited disease ch...
Tuberous sclerosis complex is an autosomal dominant disorder that can cause nonmalignant hamartomas ...
Tuberous Sclerosis Complex (TSC) is a multisystem genetic disease characterized by cutaneous and ext...
ABSTRACT: Tuberous sclerosis complex is a type of genetic multisystem disease that causes hamartomas...
Introduction: Tuberous sclerosis complex (TSC) is a rare, genetic disease that leads to neurological...
Tuberous sclerosis is a rare congenital disorder with an incidence of 1 in 6000 births. The classic ...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder resulting in the growth o...
Tuberous Sclerosis Complex is an autosomal dominant phakomatosis. This neurocutaneous disorder usual...
Tuberous sclerosis complex (TSC) is an inherited neurocutaneous disorder with multisystem involvemen...
Tuberous sclerosis complex is a genetic disease characterized by multisystemic hamartomas with varia...
Tuberous sclerosis is a rare autosomal dominant disorder. Myofibroblasts are cells with a hybrid phe...
Clinical manifestations of tuberous sclerosis (TS) are variable, and oral involvement occurs in less...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Introduction: Tuberous sclerosis complex (TSC) is a neurocutaneous syndrome produced by a number of ...