Hereditary haemorrhagic telangiectasia (Q42586): Difference between revisions
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A doença de Rendu-Osler-Weber, também chamada de telangiectasia hemorrágica hereditária (THH), é um transtorno genético da angiogênese que leva a dilatações arteriovenosas: telangiectasias mucocutâneas hemorrágicas e shunts viscerais. | |||
| description / en | description / en | ||
Rendu-Osler-Weber disease, also called hereditary haemorrhagic telangiectasia (HHT), is a genetic disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal haemorrhagic telangiectasias and visceral shunting. | |||
Revision as of 09:10, 13 August 2026
Rendu-Osler-Weber disease, also called hereditary haemorrhagic telangiectasia (HHT), is a genetic disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal haemorrhagic telangiectasias and visceral shunting.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA90.00 |
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| English | Hereditary haemorrhagic telangiectasia |
Rendu-Osler-Weber disease, also called hereditary haemorrhagic telangiectasia (HHT), is a genetic disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal haemorrhagic telangiectasias and visceral shunting. |
