Scott syndrome (Q84804): Difference between revisions
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13 August 2026
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Latest 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. |
Statements
CID11:ID_186013982
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dki-india-ID_186013982
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Concluído
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13 August 2026
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