Hereditary deficiency of factor I (Q39582): Difference between revisions
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Deficiências congênitas do fibrinogênio são distúrbios da coagulação caracterizados por manifestações hemorrágicas que variam de leves a graves, como resultado da quantidade e/ou qualidade reduzida de fibrinogênio circulante. Afibrinogenemia (ausência completa de fibrinogênio) e hipofibrinogenemia (concentração plasmática reduzida de fibrinogênio) correspondem a anomalias quantitativas do fibrinogênio, enquanto disfibrinogenemia corresponde a uma anomalia funcional do fibrinogênio. Hipo- e disfribinogenemia podem, frequentemente, coexistir (hipodisfribrinogenemia). | |||
| description / en | description / en | ||
Congenital deficiencies of fibrinogen are coagulation disorders characterised by bleeding symptoms ranging from mild to severe resulting from reduced quantity and/or quality of circulating fibrinogen. Afibrinogenaemia (complete absence of fibrinogen) and hypofibrinogenaemia (reduced plasma fibrinogen concentration) correspond to quantitative anomalies of fibrinogen while dysfibrinogenaemia corresponds to a functional anomaly of fibrinogen. Hypo- and dysfibrinogenaemia may be frequently combined (hypodysfibrinogenaemia). | |||
Revision as of 05:03, 13 August 2026
Congenital deficiencies of fibrinogen are coagulation disorders characterised by bleeding symptoms ranging from mild to severe resulting from reduced quantity and/or quality of circulating fibrinogen. Afibrinogenaemia (complete absence of fibrinogen) and hypofibrinogenaemia (reduced plasma fibrinogen concentration) correspond to quantitative anomalies of fibrinogen while dysfibrinogenaemia corresponds to a functional anomaly of fibrinogen. Hypo- and dysfibrinogenaemia may be frequently combined (hypodysfibrinogenaemia).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B14.0 |
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| English | Hereditary deficiency of factor I |
Congenital deficiencies of fibrinogen are coagulation disorders characterised by bleeding symptoms ranging from mild to severe resulting from reduced quantity and/or quality of circulating fibrinogen. Afibrinogenaemia (complete absence of fibrinogen) and hypofibrinogenaemia (reduced plasma fibrinogen concentration) correspond to quantitative anomalies of fibrinogen while dysfibrinogenaemia corresponds to a functional anomaly of fibrinogen. Hypo- and dysfibrinogenaemia may be frequently combined (hypodysfibrinogenaemia). |
