Renal angiomyolipomata associated with tuberous sclerosis complex are often bilateral, multiple and progressive. They cause significant morbidity and mortality in older children and adults. Surveillance and pre-emptive treatment reduce this risk. Recent research suggests treatment with mammalian target of rapamycin inhibitors is better at preventing bleeding, recurrence, and preserving renal function than percutaneous embolization
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
Tuberous sclerosis, caused by germline mutations in the TSC1 or TSC2 genes, is associated with aberr...
Tuberous sclerosis complex (TSC) is an autosomal-dominant multi system disorder. The genetic basis o...
Tuberous sclerosis complex is a rare multisystemic genetic disorder associated with the development ...
We present a case of a 32-year-old female who had been diagnosed tuberous sclerosis complex (TSC) tw...
Renal angiomyolipomas are found in up to 80% of tuberous sclerosis complex (TSC) patients. Although ...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder promoting the development of beni...
AbstractObjectiveTo deduce recommendations from the literature on the management of kidney damage ca...
Renal lesions represent the second most significant cause of morbidity and mortality in patients wit...
Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an estimated prevalence o...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
Abstract Background Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an es...
We report a case of misdiagnosed tuberous sclerosis complex (TSC) in a patient without TSC gene vari...
International audienceIn patients with tuberous sclerosis complex (TSC), renal complications are not...
Renal angiomyolipomata. Renal angiomyolipomata can exist as an imaging curiosity or represent a life...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
Tuberous sclerosis, caused by germline mutations in the TSC1 or TSC2 genes, is associated with aberr...
Tuberous sclerosis complex (TSC) is an autosomal-dominant multi system disorder. The genetic basis o...
Tuberous sclerosis complex is a rare multisystemic genetic disorder associated with the development ...
We present a case of a 32-year-old female who had been diagnosed tuberous sclerosis complex (TSC) tw...
Renal angiomyolipomas are found in up to 80% of tuberous sclerosis complex (TSC) patients. Although ...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder promoting the development of beni...
AbstractObjectiveTo deduce recommendations from the literature on the management of kidney damage ca...
Renal lesions represent the second most significant cause of morbidity and mortality in patients wit...
Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an estimated prevalence o...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
Abstract Background Tuberous sclerosis (TS) is a rare autosomal dominant systemic disease with an es...
We report a case of misdiagnosed tuberous sclerosis complex (TSC) in a patient without TSC gene vari...
International audienceIn patients with tuberous sclerosis complex (TSC), renal complications are not...
Renal angiomyolipomata. Renal angiomyolipomata can exist as an imaging curiosity or represent a life...
Renal-related disease is the most common cause of tuberous sclerosis complex (TSC)-related death in ...
Tuberous sclerosis, caused by germline mutations in the TSC1 or TSC2 genes, is associated with aberr...
Tuberous sclerosis complex (TSC) is an autosomal-dominant multi system disorder. The genetic basis o...