Hereditary hypofibrinogenaemia (Q68728): Difference between revisions
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Hipofibrinogenemia familiar é um transtorno da coagulação caracterizado por sintomas leves de sangramentos subsequentes a traumatismo ou cirurgia devido a concentração reduzida de fibrinogênio plasmático. | |||
| description / en | description / en | ||
Familial hypofibrinogenemia is a coagulation disorder characterised by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration. | |||
Revision as of 16:46, 14 August 2026
Familial hypofibrinogenemia is a coagulation disorder characterised by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_559585471 |
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| English | Hereditary hypofibrinogenaemia |
Familial hypofibrinogenemia is a coagulation disorder characterised by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration. |
