Awidi A S
Scand J Haematol. 1983 Mar;30(3):218-22. doi: 10.1111/j.1600-0609.1983.tb01477.x.
12 Jordanian patients from 9 families with Glanzmann's thrombasthenia are described. All of them are products of consanguinous marriages. All cases are children with varying severity of mucosal bleeding. The clinical and laboratory findings are described. The importance of consanguinity is discussed and emphasized. Glanzmann's thrombasthenia is the second most common inherited haemorrhagic disorder in Jordan.
本文描述了来自9个家庭的12名患有Glanzmann血小板无力症的约旦患者。他们均为近亲结婚的后代。所有病例均为儿童，有不同程度的黏膜出血。文中描述了临床和实验室检查结果。讨论并强调了近亲结婚的重要性。Glanzmann血小板无力症是约旦第二常见的遗传性出血性疾病。
