Atresia of oesophagus (Q46311): Difference between revisions
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13 August 2026
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Latest revision as of 14:48, 13 August 2026
Oesophageal atresia encompasses a group of congenital anomalies with an interruption in the continuity of the oesophagus, with or without persistent communication with the trachea. In 86% of cases there is a distal tracheoesophageal fistula, in 7% of cases there is no fistulous connection, while in 4% of cases there is a tracheoesophageal fistula without atresia. The remaining cases are made up of patients with OA with proximal, or both proximal and distal, tracheoesophageal fistula.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB12.1 |
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| English | Atresia of oesophagus |
Oesophageal atresia encompasses a group of congenital anomalies with an interruption in the continuity of the oesophagus, with or without persistent communication with the trachea. In 86% of cases there is a distal tracheoesophageal fistula, in 7% of cases there is no fistulous connection, while in 4% of cases there is a tracheoesophageal fistula without atresia. The remaining cases are made up of patients with OA with proximal, or both proximal and distal, tracheoesophageal fistula. |
Statements
CID11:LB12.1
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dki-india-LB12.1
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Concluído
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13 August 2026
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