Scott syndrome (Q84804): Difference between revisions
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Síndrome de Scott é um transtorno hemorrágico extremamente raro caracterizado por episódios de hemorragia explicados por um comprometimento na atividade procoagulante expressada pelas plaquetas ativadas, que são incapazes de expor fosfolípides aniônicos e de liberar micropartículas procoagulantes. | |||
| description / en | description / en | ||
Scott syndrome is an extremely rare haemorrhagic disorder characterised by haemorrhagic episodes explained by an impairment of the procoagulant activity expressed by stimulated platelets, which are unable to expose anionic phospholipids and to shed procoagulant microparticles. | |||
Revision as of 10:09, 15 August 2026
Scott syndrome is an extremely rare haemorrhagic disorder characterised by haemorrhagic episodes explained by an impairment of the procoagulant activity expressed by stimulated platelets, which are unable to expose anionic phospholipids and to shed procoagulant microparticles.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_186013982 |
||
| English | Scott syndrome |
Scott syndrome is an extremely rare haemorrhagic disorder characterised by haemorrhagic episodes explained by an impairment of the procoagulant activity expressed by stimulated platelets, which are unable to expose anionic phospholipids and to shed procoagulant microparticles. |
