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血小板无力症 (ｇｌａｎｚｍａｎｎｔｈｒｏｍｂａｓｔｈｅｎｉａ,ＧＴ)为遗传性血小板功能缺陷中最为常见的疾病 ,是血小板膜糖蛋白Ⅱｂ/Ⅲａ(ＧＰⅡｂ/Ⅲａ)数量减少或结构异常所致的出血性疾病[1] 。下面根据 1986年修定后的标准诊断总结我科 1983～ 1999年门诊及病房共 2 2
Glanzmann thrombasthenia (GT) is the most common disease of hereditary platelet function defect and is a hemorrhagic disease caused by a decrease in the number of platelet glycoprotein Ⅱb / Ⅲa (GPⅡb / Ⅲa) or structural abnormalities [1]. The following according to the 1986 revised standard diagnostic summary of our department from 1983 to 1999 outpatient and ward a total of 2 2