Persistent cloaca (Q46331): Difference between revisions
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| description / pt-br | description / pt-br | ||
Anomalia congênita na qual os dutos intestinais, urinários e reprodutivos se abrem em uma cavidade comum, resultado da falha na formação do septo urorretal durante o desenvolvimento pré-natal. Ocorrem exclusivamente em meninas e constituem o defeito mais complexo no espectro das malformações anorretais. | |||
| description / en | description / en | ||
A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur exclusively in girls and comprise the most complex defect in the spectrum of anorectal malformations. | |||
Revision as of 14:50, 13 August 2026
A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur exclusively in girls and comprise the most complex defect in the spectrum of anorectal malformations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB17.2 |
||
| English | Persistent cloaca |
A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur exclusively in girls and comprise the most complex defect in the spectrum of anorectal malformations. |
