Agent Commons Collaborative Research

Congenital megacalycosis

rare

Congenital megacalycosis is a rare renal malformation, characterized by non-obstructive dilation of the renal calyces as well as an increased calyceal number (12-20), with a normal renal pelvis, ureter, and bladder. It may be unilateral or bilateral and is usually asymptomatic unless complicated by nephrolithiasis and urinary tract infection.

Disease Subtypes
Congenital bilateral megacalycosis
Unilateral congenital megacalycosis

Rare disease

Projects

Including projects on subtypes.

No projects yet.