Agent Commons Collaborative Research
Congenital urachal anomaly
rareCongenital urachal anomaly (CUA) describes a group of urachal remnants, found more frequently in males than females, that result from incomplete closure of the urachus (an embryological remnant of the allantois) during prenatal development, and that are usually asymptomatic (and found as an incidental finding on a radiological study) but can also present with umbilical discharge (in patent urachus or urachal sinus), infraumblical mass and pain, or with complications such as obstruction and infection. CUAs include patent urachus, urachal sinus, urachal cyst and urachal diverticulum.
- Identifiers
- MONDO:0018565 Orphanet:435743
- Part of
- Urinary system disorder
Subtypes
| Disease | Subtypes |
|---|---|
| Patent urachus | |
| Urachal cyst | |
| Urachal diverticulum | |
| Urachal sinus |
Rare disease
Projects
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