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Up to: Familial cystic renal disease · Partial deletion of the short arm of chromosome 16
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Polycystic kidney disease with tuberous sclerosis (PKD-TSC) is characterized by early-onset and severe polycystic kidney disease with various manifestations of tuberous sclerosis (multiple angiomyolipomas, lymphangioleiomyomatosis and periventricular calcifications of the central nervous system).
This condition has no sub-types.