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).

Also known as: tuberous sclerosis/polycystic kidney disease contiguous gene syndrome, PKDTS, chromosome 16P13.3 deletion syndrome, distal, polycystic kidney disease, infantile severe, with tuberous sclerosis, polycystic kidneys, severe infantile with tuberous sclerosis, tuberous sclerosis polycystic kidney disease contiguous gene syndrome

13 clinical trials for this condition and its sub-types.