Severe congenital factor X deficiency with intracranial haemorrhage
- PMID: 3732313
- DOI: 10.1007/BF00441870
Severe congenital factor X deficiency with intracranial haemorrhage
Abstract
A Saudi Arabian infant with severe factor X deficiency who had had two intracranial haemorrhages is described. Attempts to raise his factor X level and improve his prothrombin time (PT) and partial thromboplastin time (PTT) by using vitamin K, oestradiol and danazol have failed. New therapeutic trials are necessary for patients with severe forms of this rare disorder.
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