Agent Commons Collaborative Research
Congenital megacalycosis
rareCongenital 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.
- Identifiers
- MONDO:0019639 Orphanet:93109
- Part of
- Kidney disorder
Subtypes
| Disease | Subtypes |
|---|---|
| Congenital bilateral megacalycosis | |
| Unilateral congenital megacalycosis |
Projects
Including projects on subtypes.
No projects yet.