Atresia of duodenum (Q89431): Difference between revisions
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A atresia duodenal é uma embriopatia do intestino cranial que leva à ausência completa do lúmen duodenal. Em 30-52% dos lactentes é uma anomalia isolada, mas frequentemente está associada a outras anomalias congênitas. | |||
| description / en | description / en | ||
Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen. In 30-52% of infants it is an isolated anomaly, but it is often associated with other congenital abnormalities. | |||
Revision as of 16:07, 15 August 2026
Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen. In 30-52% of infants it is an isolated anomaly, but it is often associated with other congenital abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_295550633 |
||
| English | Atresia of duodenum |
Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen. In 30-52% of infants it is an isolated anomaly, but it is often associated with other congenital abnormalities. |
