Sporadic primary achalasia (Q101592): Difference between revisions
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Tipo comum de transtorno de motilidade esofágica de acalasia primária não hereditária, envolvendo a camada de músculo liso do esôfago e o esfíncter esofágico inferior (EEI) na ausência de outras explicações como câncer ou fibrose. | |||
| description / en | description / en | ||
This is a common type of oesophageal motility disorder of non-inherited form of primary achalasia, involving the smooth muscle layer of the oesophagus and the lower oesophageal sphincter (LES) in the absence of other explanations like cancer or fibrosis. | |||
Revision as of 18:25, 16 August 2026
This is a common type of oesophageal motility disorder of non-inherited form of primary achalasia, involving the smooth muscle layer of the oesophagus and the lower oesophageal sphincter (LES) in the absence of other explanations like cancer or fibrosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_505440999 |
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| English | Sporadic primary achalasia |
This is a common type of oesophageal motility disorder of non-inherited form of primary achalasia, involving the smooth muscle layer of the oesophagus and the lower oesophageal sphincter (LES) in the absence of other explanations like cancer or fibrosis. |
