Congenital megacalycosis

MONDO:0019639

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.

0 clinical trials for this condition and its sub-types, 0 tagged with Congenital megacalycosis itself.

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↑ Kidney disorder (4032)

Sub-types of Congenital megacalycosis

Congenital bilateral megacalycosis 0 trials
Unilateral congenital megacalycosis 0 trials

Including sub-types (0) Tagged with Congenital megacalycosis (0)

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