Shaikh A N, Khurshid M
Department of Pathology, Aga Khan University Hospital, Karachi.
J Pak Med Assoc. 1993 Apr;43(4):67-9.
Patients with undiagnosed haemostatic defects seen at The Aga Khan Hospital and Fatimid Blood Transfusion Centre during the period of 7 years (1985-1992) were screened with routine tests including bleeding time (BT), whole blood clotting time (CT), platelet count, activated partial thromboplastin time (APTT), prothrombin time (PT) and 5 molar urea test. Nine patients had a positive 5 molar urea test indicating factor XIII deficiency. Rest of the screening tests were normal in these patients. High incidence of consanguinity was observed in affected families. Clinical features included excessive bleeding from umbilical stump, bruising, post-traumatic bleeding, epistaxis, melaena and intracerebral bleeding. All the patients were treated with fresh frozen plasma and cryoprecipitate.
在7年期间(1985 - 1992年),于阿迦汗医院和法蒂玛输血中心就诊的未确诊止血缺陷患者,接受了包括出血时间(BT)、全血凝固时间(CT)、血小板计数、活化部分凝血活酶时间(APTT)、凝血酶原时间(PT)和5摩尔尿素试验在内的常规检查。9名患者的5摩尔尿素试验呈阳性,提示因子XIII缺乏。这些患者的其余筛查试验均正常。在受影响的家庭中观察到近亲结婚的高发生率。临床特征包括脐带残端出血过多、瘀伤、创伤后出血、鼻出血、黑便和脑出血。所有患者均接受了新鲜冰冻血浆和冷沉淀治疗。