Ahmed M A, Al-Sohaibani M O, Al-Mohaya S A, Sumer T, Al-Sheikh E H, Knox-Macaulay H
King Fahd Hospital of University, Dammam, Saudi Arabia.
Acta Haematol. 1988;79(4):202-6. doi: 10.1159/000205808.
Thirty-four cases of inherited bleeding disorders are reported. All are Saudi patients from the Eastern Province of Saudi Arabia. There were 15 haemophiliacs, 1 factor VII deficiency, 1 factor X deficiency, 12 Glanzmann's thrombasthenia, and 5 unidentified platelet function disorders. Consanguinity was common among the families of these patients. Different age groups were affected and the severity of bleeding varied in the different conditions reported.
报告了34例遗传性出血性疾病病例。所有患者均为来自沙特阿拉伯东部省的沙特人。其中有15例血友病患者、1例因子VII缺乏症患者、1例因子X缺乏症患者、12例血小板无力症患者以及5例不明原因的血小板功能障碍患者。这些患者的家族中近亲结婚现象很常见。不同年龄组均受影响，且所报告的不同病症中出血严重程度各异。
