Fibrinolytic defects (Q52735): Difference between revisions
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Doença causada por determinantes que surgem durante o período pré-natal, após o nascimento ou por fatores geneticamente determinados, afetando o sistema fibrinolítico, que evita que coágulos sanguíneos se estendam e se tornem problemáticos. Essa doença é caracterizada por defeitos no sistema fibrinolítico levando a coagulação do sangue. Pode apresentar-se com trombose. | |||
| description / en | description / en | ||
A disease caused by determinants arising during the antenatal period, after birth or genetically inherited factors, affecting the fibrinolysis system which prevents blood clots from growing and becoming problematic. This disease is characterised by defects in the fibrinolysis system leading to coagulation of the blood. This disease may present with thrombosis. | |||
Revision as of 00:03, 14 August 2026
A disease caused by determinants arising during the antenatal period, after birth or genetically inherited factors, affecting the fibrinolysis system which prevents blood clots from growing and becoming problematic. This disease is characterised by defects in the fibrinolysis system leading to coagulation of the blood. This disease may present with thrombosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1881300992 |
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| English | Fibrinolytic defects |
A disease caused by determinants arising during the antenatal period, after birth or genetically inherited factors, affecting the fibrinolysis system which prevents blood clots from growing and becoming problematic. This disease is characterised by defects in the fibrinolysis system leading to coagulation of the blood. This disease may present with thrombosis. |
