We report a case of misdiagnosed tuberous sclerosis complex (TSC) in a patient without TSC gene variant presenting with bilateral renal angiomyolipomas and seizures in the context of strong family history of polycystic kidney disease. Clinical diagnosis of tuberous sclerosis complex was made and treatment with everolimus reduced size of renal angiomyolipomas. In this case, report we discuss the association between tuberous sclerosis complex and polycystic kidney disease and novel treatment for TSC
Tuberous sclerosis (TS) is a relatively rare multi-organ disorder generally diagnosed in infancy and...
Tuberous sclerosis complex is a genetic (autosomal dominant) disorder affecting cellular differentia...
PubMedID: 15074379Tuberous sclerosis complex is an autosomal dominant disorder of cellular prolifera...
Tuberous sclerosis complex is a rare multisystemic genetic disorder associated with the development ...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder with a birth incidence of...
A case of a 37-year old man affected by tuberous sclerosis with bilateral renal angiomyolipomas is d...
Tuberous sclerosis complex (TSC) is a multisystem disorder, with significant renal cystic and solid ...
Abstract Tuberous sclerosis is a common life long disease requiring long-term follow-up. It is well ...
Tuberous sclerosis complex is a genetic disorder characterized by hamartomatous lesions in multiple ...
Renal angiomyolipomata associated with tuberous sclerosis complex are often bilateral, multiple and ...
Tuberous sclerosis complex (TSC) is an autosomal-dominant multi system disorder. The genetic basis o...
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...
Tuberous sclerosis is a multiple system disease, involving the brain, skin, kidneys, heart and other...
Abstract Background Tuberous sclerosis complex is an autosomal dominant genetic disorder that affect...
Tuberous sclerosis (TS) is a relatively rare multi-organ disorder generally diagnosed in infancy and...
Tuberous sclerosis complex is a genetic (autosomal dominant) disorder affecting cellular differentia...
PubMedID: 15074379Tuberous sclerosis complex is an autosomal dominant disorder of cellular prolifera...
Tuberous sclerosis complex is a rare multisystemic genetic disorder associated with the development ...
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder with a birth incidence of...
A case of a 37-year old man affected by tuberous sclerosis with bilateral renal angiomyolipomas is d...
Tuberous sclerosis complex (TSC) is a multisystem disorder, with significant renal cystic and solid ...
Abstract Tuberous sclerosis is a common life long disease requiring long-term follow-up. It is well ...
Tuberous sclerosis complex is a genetic disorder characterized by hamartomatous lesions in multiple ...
Renal angiomyolipomata associated with tuberous sclerosis complex are often bilateral, multiple and ...
Tuberous sclerosis complex (TSC) is an autosomal-dominant multi system disorder. The genetic basis o...
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...
Tuberous sclerosis is a multiple system disease, involving the brain, skin, kidneys, heart and other...
Abstract Background Tuberous sclerosis complex is an autosomal dominant genetic disorder that affect...
Tuberous sclerosis (TS) is a relatively rare multi-organ disorder generally diagnosed in infancy and...
Tuberous sclerosis complex is a genetic (autosomal dominant) disorder affecting cellular differentia...
PubMedID: 15074379Tuberous sclerosis complex is an autosomal dominant disorder of cellular prolifera...