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

• मुख्य लेखकों: T P Vigneshwaran (लेखक), A R Mullai Baalaaji (लेखक), S Ashok Kumar (लेखक), D Ashwath (लेखक), Thirugnanam Rajasekar (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: Wolters Kluwer Medknow Publications, 2018-01-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: 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...