Congenital stenosis or stricture of oesophagus (Q46315): Difference between revisions
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| description / pt-br | description / pt-br | ||
Uma forma de obstrução esofágica incompleta devida a um defeito de desenvolvimento do intestino anterior primitivo. O estreitamento anormal do esôfago ocorre mais frequentemente na junção dos terços médio e inferior. As manifestações clínicas, aparentes 2 a 3 semanas após o nascimento, incluem disfagia e vômitos progressivos. | |||
| description / en | description / en | ||
A form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut. Abnormal narrowing of the oesophagus occurs most often at the junction of the middle and lower thirds. Clinical manifestations, apparent 2 to 3 weeks after birth, include dysphagia and progressive vomiting. | |||
Revision as of 14:48, 13 August 2026
A form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut. Abnormal narrowing of the oesophagus occurs most often at the junction of the middle and lower thirds. Clinical manifestations, apparent 2 to 3 weeks after birth, include dysphagia and progressive vomiting.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LB12.3 |
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| English | Congenital stenosis or stricture of oesophagus |
A form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut. Abnormal narrowing of the oesophagus occurs most often at the junction of the middle and lower thirds. Clinical manifestations, apparent 2 to 3 weeks after birth, include dysphagia and progressive vomiting. |
