BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome causing hamartomatous growths in multiple organs. Facial angiofibromas occur in up to 80% of patients and can be highly disfiguring. Treatment for these lesions has historically been challenging. Recently, topical rapamycin has been proposed as an effective option to treat angiofibromas but a commercially available compound has not yet been developed. OBJECTIVES: The aim of this review is to analyse the current data on the use of topical rapamycin in the treatment of angiofibromas in TSC, focusing on the risk-benefit profile. METHODS: A retrospective review of the English-language literature was conducted. RESULTS: Sixteen reports describing th...
Tuberous Sclerosis Complex (TSC) is a rare autosomal dominant genetic disease caused by a deactivati...
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder with an incidence...
Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an estimated prevalence o...
BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome causi...
Abstract Background and Objectives: Facial angiofibromas are disfiguring facial lesions, present in ...
The use of topical rapamycin or rapalog, an mTOR inhibitor, has shown promising results in treating ...
Aim: Topical rapamycin for angiofibromas has been reported to be a new promising treatment. This stu...
Facial angiofibromas, composed of fibrous tissue and blood vessels appearing on the face, are closel...
Background and Objectives: Facial angiofibromas are disfiguring facial lesions, present in up to 80%...
Tuberous sclerosis complex (TSC) is a neurocutaneus disease that causes various other tumors includi...
BACKGROUND: Recent reports have suggested that the topical formulation of sirolimus is effective...
Background: The skin is one of the most affected organs in tuberous sclerosis complex and angiofibro...
Facial angiofibromas are dermatological manifestations of tuberous sclerosis complex, a neurocutaneo...
<b><i>Background:</i></b> Recent reports have suggested that the topical formulation of sirolimus is...
<p><b>Article full text</b></p> <p><br></p> <p>The full text of this article can be found here<b>....
Tuberous Sclerosis Complex (TSC) is a rare autosomal dominant genetic disease caused by a deactivati...
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder with an incidence...
Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an estimated prevalence o...
BACKGROUND: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome causi...
Abstract Background and Objectives: Facial angiofibromas are disfiguring facial lesions, present in ...
The use of topical rapamycin or rapalog, an mTOR inhibitor, has shown promising results in treating ...
Aim: Topical rapamycin for angiofibromas has been reported to be a new promising treatment. This stu...
Facial angiofibromas, composed of fibrous tissue and blood vessels appearing on the face, are closel...
Background and Objectives: Facial angiofibromas are disfiguring facial lesions, present in up to 80%...
Tuberous sclerosis complex (TSC) is a neurocutaneus disease that causes various other tumors includi...
BACKGROUND: Recent reports have suggested that the topical formulation of sirolimus is effective...
Background: The skin is one of the most affected organs in tuberous sclerosis complex and angiofibro...
Facial angiofibromas are dermatological manifestations of tuberous sclerosis complex, a neurocutaneo...
<b><i>Background:</i></b> Recent reports have suggested that the topical formulation of sirolimus is...
<p><b>Article full text</b></p> <p><br></p> <p>The full text of this article can be found here<b>....
Tuberous Sclerosis Complex (TSC) is a rare autosomal dominant genetic disease caused by a deactivati...
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder with an incidence...
Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an estimated prevalence o...