AbstractObjectiveTo deduce recommendations from the literature on the management of kidney damage caused by tuberous sclerosis complex (TSC).Material and methodsFive practitioners have written up recommendations after reviewing the literature. They were evaluated by 14 experts using a 9 level scale (1: complete disagreement; 9: complete agreement), then reworded until each item received a median score of greater than or equal to 8.ResultsForty-eight to 80% of patients with TSC have kidney disease with the presence of angiomyolipomas (AML), cysts, cancers and/or progression towards renal insufficiency. An abdominal ultrasound (and serum creatinine level if there is an abnormality) is recommended as soon as the TSC is diagnosed. The evaluatio...
Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an estimated prevalence o...
BackgroundLong-term data from patients with tuberous sclerosis complex (TSC)-associated renal angiom...
Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem genetic disorder characterized...
AbstractObjectiveTo deduce recommendations from the literature on the management of kidney damage ca...
Renal angiomyolipomas are found in up to 80% of tuberous sclerosis complex (TSC) patients. Although ...
Tuberous sclerosis complex is a genetic disorder characterized by hamartomatous lesions in multiple ...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
ObjectiveTo estimate the incidence rates of kidney-related clinical outcomes among patients with tub...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
International audienceIn patients with tuberous sclerosis complex (TSC), renal complications are not...
Tuberous sclerosis (TS) otozomal dominant geçişli, birçok organ sisteminde hamartomlarla karakterize...
Renal lesions represent the second most significant cause of morbidity and mortality in patients wit...
Background Renal angiomyolipomas (AMLs) are a major clinical feature in patients wit...
Introduction: About 20% of renal angiomyolipomas (RAML) are associated with tuberous sclerosis compl...
Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an estimated prevalence o...
BackgroundLong-term data from patients with tuberous sclerosis complex (TSC)-associated renal angiom...
Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem genetic disorder characterized...
AbstractObjectiveTo deduce recommendations from the literature on the management of kidney damage ca...
Renal angiomyolipomas are found in up to 80% of tuberous sclerosis complex (TSC) patients. Although ...
Tuberous sclerosis complex is a genetic disorder characterized by hamartomatous lesions in multiple ...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
ObjectiveTo estimate the incidence rates of kidney-related clinical outcomes among patients with tub...
Tuberous sclerosis complex (TSC) is a genetic condition caused by a mutation in either the TSC1 or T...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
International audienceIn patients with tuberous sclerosis complex (TSC), renal complications are not...
Tuberous sclerosis (TS) otozomal dominant geçişli, birçok organ sisteminde hamartomlarla karakterize...
Renal lesions represent the second most significant cause of morbidity and mortality in patients wit...
Background Renal angiomyolipomas (AMLs) are a major clinical feature in patients wit...
Introduction: About 20% of renal angiomyolipomas (RAML) are associated with tuberous sclerosis compl...
Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an estimated prevalence o...
BackgroundLong-term data from patients with tuberous sclerosis complex (TSC)-associated renal angiom...
Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem genetic disorder characterized...