Hereditary factor VII deficiency (Q89789): Difference between revisions
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A deficiência do fator VII (FVII) é uma doença hemorrágica hereditária rara causada pela diminuição ou ausência desse fator da coagulação. A expressão clínica dessa doença é bastante variável, e nenhuma relação consistente entre a gravidade da síndrome hemorrágica e os níveis residuais de atividade do fator VII foi encontrada. | |||
| description / en | description / en | ||
Factor VII (FVII) deficiency is a rare hereditary haemorrhagic disease caused by the diminution or absence of this coagulation factor. The clinical expression of this disorder is highly variable, and no consistent relationship has been found between the severity of the haemorrhagic syndrome and the residual levels of FVII activity. | |||
Revision as of 16:37, 15 August 2026
Factor VII (FVII) deficiency is a rare hereditary haemorrhagic disease caused by the diminution or absence of this coagulation factor. The clinical expression of this disorder is highly variable, and no consistent relationship has been found between the severity of the haemorrhagic syndrome and the residual levels of FVII activity.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2034923927 |
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| English | Hereditary factor VII deficiency |
Factor VII (FVII) deficiency is a rare hereditary haemorrhagic disease caused by the diminution or absence of this coagulation factor. The clinical expression of this disorder is highly variable, and no consistent relationship has been found between the severity of the haemorrhagic syndrome and the residual levels of FVII activity. |
