Severe congenital factor X deficiency - An unusual cause of intracranial hemorrhage

• Hoofdauteurs: T P Vigneshwaran (Auteur), A R Mullai Baalaaji (Auteur), S Ashok Kumar (Auteur), D Ashwath (Auteur), Thirugnanam Rajasekar (Auteur)
• Formaat: Boek
• Gepubliceerd in: Wolters Kluwer Medknow Publications, 2018-01-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

Factor X deficiency is one of the rare inherited coagulation disorders. Symptoms vary from mild to severe with the commonest being epistaxis, gum bleeds and menorrhagia. The diagnosis is suspected when both PT and aPTT are prolonged and remains uncorrected following Vitamin K administration. Replace...