Triple A syndrome (Q90864): Difference between revisions
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| description / pt-br | description / pt-br | ||
Síndrome triplo A é um transtorno autossômico recessivo caracterizado pela tríade de resistência ao hormônio adrenocorticotrófico (ACTH), acalasia (hipertrofia da cárdia gastroesofágica, impedindo que os alimentos entrem no estômago) e alacrimia (ausência de lágrimas). | |||
| description / en | description / en | ||
Triple A syndrome is an autosomal recessive disorder characterised by the triad of adrenocorticotropic hormone (ACTH) resistant adrenal insufficiency, achalasia (hypertrophy of the gastroesophageal cardia, preventing food from entering the stomach), and alacrima (absence of tears). | |||
Revision as of 17:51, 15 August 2026
Triple A syndrome is an autosomal recessive disorder characterised by the triad of adrenocorticotropic hormone (ACTH) resistant adrenal insufficiency, achalasia (hypertrophy of the gastroesophageal cardia, preventing food from entering the stomach), and alacrima (absence of tears).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_180128195 |
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| English | Triple A syndrome |
Triple A syndrome is an autosomal recessive disorder characterised by the triad of adrenocorticotropic hormone (ACTH) resistant adrenal insufficiency, achalasia (hypertrophy of the gastroesophageal cardia, preventing food from entering the stomach), and alacrima (absence of tears). |
