Congenital oesophageal web or ring (Q46316): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Forma rara de obstrução esofágica incompleta devida a um defeito de desenvolvimento do intestino anterior primitivo, que se apresenta como uma lesão da mucosa formando um diafragma incompleto. Os sintomas (aparentes desde o nascimento) incluem disfagia, regurgitação e engasgos. | |||
| description / en | description / en | ||
A rare form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut that presents as a mucosal lesion forming an incomplete diaphragm. Symptoms (apparent from birth) include dysphagia, regurgitation, and choking. | |||
Revision as of 14:48, 13 August 2026
A rare form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut that presents as a mucosal lesion forming an incomplete diaphragm. Symptoms (apparent from birth) include dysphagia, regurgitation, and choking.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB12.0 |
||
| English | Congenital oesophageal web or ring |
A rare form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut that presents as a mucosal lesion forming an incomplete diaphragm. Symptoms (apparent from birth) include dysphagia, regurgitation, and choking. |
