Moderately severe haemophilia B (Q89199): Difference between revisions

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Hemofilia B moderadamente grave é uma forma de hemofilia B (veja este termo), caracterizada pela deficiência de fator IX, levando a sangramento anormal como resultado de ferimentos menores ou subsequente a cirurgias ou extrações dentárias. Hemofilia B moderadamente grave responde por cerca de 30% de todos os casos de hemofilia B. A atividade biológica do fator IX encontra-se entre 1% e 5%. Hemorragias espontâneas são raras. A transmissão é recessiva ligada ao X, e o transtorno é causado por mutações no gene F9 (Xq28), que codifica o fator IX da coagulação.
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Moderately severe haemophilia B is a form of haemophilia B (see this term) characterised by factor IX deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Moderately severe haemophilia B accounts for around 30% of all cases of haemophilia B. The biological activity of factor IX is between 1% and 5%. Spontaneous haemorrhages are rare. Transmission is X-linked recessive and the disorder is caused by mutations in the F9 gene (Xq28) encoding coagulation factor IX.

Revision as of 15:46, 15 August 2026

Moderately severe haemophilia B is a form of haemophilia B (see this term) characterised by factor IX deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Moderately severe haemophilia B accounts for around 30% of all cases of haemophilia B. The biological activity of factor IX is between 1% and 5%. Spontaneous haemorrhages are rare. Transmission is X-linked recessive and the disorder is caused by mutations in the F9 gene (Xq28) encoding coagulation factor IX.
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    Moderately severe haemophilia B
    Moderately severe haemophilia B is a form of haemophilia B (see this term) characterised by factor IX deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Moderately severe haemophilia B accounts for around 30% of all cases of haemophilia B. The biological activity of factor IX is between 1% and 5%. Spontaneous haemorrhages are rare. Transmission is X-linked recessive and the disorder is caused by mutations in the F9 gene (Xq28) encoding coagulation factor IX.

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