Moderately severe haemophilia A (Q85316): Difference between revisions

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Hemofilia A moderadamente grave é uma forma de hemofilia A (veja este termo), caracterizada pela deficiência de fator VIII, levando a sangramento anormal como resultado de ferimentos menores ou subsequente a cirurgias ou extrações dentárias. Hemofilia A moderadamente grave responde por cerca de 20% de todos os casos de hemofilia A. A atividade biológica do fator VIII encontra-se entre 1% e 5%. Hemorragias espontâneas são raras. A transmissão é recessiva ligada ao X, e o transtorno é cuasado por mutações no gene F8 (Xq28), que codifica o fator VIII da coagulação.
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Moderately severe haemophilia A is a form of haemophilia A (see this term) characterised by factor VIII deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Moderately severe haemophilia A accounts for around 20% of all cases of haemophilia A. The biological activity of factor VIII is between 1% and 5%. Spontaneous haemorrhages are rare. Transmission is X-linked recessive and the disorder is caused by mutations in the F8 gene (Xq28) encoding coagulation factor VIII.

Revision as of 10:40, 15 August 2026

Moderately severe haemophilia A is a form of haemophilia A (see this term) characterised by factor VIII deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Moderately severe haemophilia A accounts for around 20% of all cases of haemophilia A. The biological activity of factor VIII is between 1% and 5%. Spontaneous haemorrhages are rare. Transmission is X-linked recessive and the disorder is caused by mutations in the F8 gene (Xq28) encoding coagulation factor VIII.
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    Moderately severe haemophilia A
    Moderately severe haemophilia A is a form of haemophilia A (see this term) characterised by factor VIII deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction. Moderately severe haemophilia A accounts for around 20% of all cases of haemophilia A. The biological activity of factor VIII is between 1% and 5%. Spontaneous haemorrhages are rare. Transmission is X-linked recessive and the disorder is caused by mutations in the F8 gene (Xq28) encoding coagulation factor VIII.

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