Tuberous sclerosis complex (TSC) is an inherited neurocutaneous disorder with multisystem involvement and highly variable expression of the disease. Common cutaneous manifestations include angiofibromas, periungual fibroma, ash-leaf-shaped macules and shagreen patch which is slightly elevated soft skin-coloured plaque usually found in lumbosacral region. We report a case of TSC in a 21- year- old Saudi man with a 13 years history of asymptomatic skin lesions and generalized tonic-clonic seizures. Dermatological examination revealed facial angiofibromas, ash leaf macules, pedunculated fibromas on trunk, and shagreen patch on the back. Scalp swelling was found and confirmed to be shagreen patch by the histopathology findings. In conclusion, ...
We report a case of tuberous sclerosis in a 19 years old teenage patient with generalized tonic-clon...
AbstractA 35-year-old man presented with dilated cardiomyopathy, an unusual association with tuberou...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...
Tuberous Sclerosis Complex is an autosomal dominant phakomatosis. This neurocutaneous disorder usual...
Tuberous Sclerosis Complex (TSC) is a neurocutaneous disorder characterised by hamartoma formation i...
Tuberous sclerosis is a genetic multisystem disorder characterized by widespread hamartomas in sever...
Tuberous Sclerosis Complex (TSC) is a multisystem genetic disease characterized by cutaneous and ext...
Tuberous sclerosis complex (TSC) is a neurocutaneous disease inherited in an autosomal dominant patt...
Background: Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by the ...
Introduction: tuberous sclerosis complex (TSC) is a neurocutaneous syndrome autosomal dominant (AD),...
Background: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disease result...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Tuberous sclerosis is a rare genetic multisystem disorder that is typically apparent shortly after b...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic neurocutaneous disorder, with hete...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder resulting in the growth o...
We report a case of tuberous sclerosis in a 19 years old teenage patient with generalized tonic-clon...
AbstractA 35-year-old man presented with dilated cardiomyopathy, an unusual association with tuberou...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...
Tuberous Sclerosis Complex is an autosomal dominant phakomatosis. This neurocutaneous disorder usual...
Tuberous Sclerosis Complex (TSC) is a neurocutaneous disorder characterised by hamartoma formation i...
Tuberous sclerosis is a genetic multisystem disorder characterized by widespread hamartomas in sever...
Tuberous Sclerosis Complex (TSC) is a multisystem genetic disease characterized by cutaneous and ext...
Tuberous sclerosis complex (TSC) is a neurocutaneous disease inherited in an autosomal dominant patt...
Background: Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by the ...
Introduction: tuberous sclerosis complex (TSC) is a neurocutaneous syndrome autosomal dominant (AD),...
Background: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disease result...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Tuberous sclerosis is a rare genetic multisystem disorder that is typically apparent shortly after b...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic neurocutaneous disorder, with hete...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder resulting in the growth o...
We report a case of tuberous sclerosis in a 19 years old teenage patient with generalized tonic-clon...
AbstractA 35-year-old man presented with dilated cardiomyopathy, an unusual association with tuberou...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...