Familial intracranial haemorrhage due to factor V deficiency.

نویسندگان

  • R S Wadia
  • S A Sangle
  • S Kripalaney
  • M Bafna
  • S R Karve
چکیده

Strokes may occur with a large number of genetic disorders. Natowicz and Kelley have reviewed the single gene disorders capable of causing familial haemorrhagic strokes. These may be classified into four groups: a) hereditary disorders affecting clotting factors or platelets; b) hereditary disease producing vascular anomaly; c) hereditary disease causing hypertension and d) miscellaneous group including neurofibromatosis, sickle cell disease and tuberous sclerosis.

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Characteristics of six newborn infants with postnatal findings of severe intracranial haemorrhage.

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01 Hepatitis B(combined)

Factor VII deficiency is a rare congenital blood disorder. Its clinical features are rather variable and ranges from epistaxis to massive intracranial haemorrhage. Treatment involves replacement therapy, which constitutes use of fresh frozen plasma, prothrombin complex concentrates or recombinant activated factor VII. Although it is a rare entity, one still needs to consider it as a probable di...

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Vitamin K Deficiency Bleeding: A Case Revealed by Intracranial Haemorrhage

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عنوان ژورنال:
  • Journal of neurology, neurosurgery, and psychiatry

دوره 55 3  شماره 

صفحات  -

تاریخ انتشار 1992