Bello A, Dorantes S, Enriqueta Zamudio M, Alvarez Amaya C, Killnee M S
Bol Med Hosp Infant Mex. 1975 Mar-Apr;32(2):227-48.
Thirty-two patients with hereditary hemorrhagic diseases and a platelet functional abnormality were set apart from our group of patients with hereditary hemorrhagic diseases, and their symptoms, signs and hematological examinations were collected; the initial events and the age of the patients when they were obsserved, the main hemorrhagic manifestations during their clinical course, the clinical severity of the disorders, the survival of the patients and the laboratory test for hemostasis useful to make the diagnosis, were evaluated. In reference to bleeding time, thirty patients had abnormal bleeding time, but the other two had normal bleeding time.
32例患有遗传性出血性疾病且存在血小板功能异常的患者从我们的遗传性出血性疾病患者组中分离出来,收集了他们的症状、体征和血液学检查结果;评估了首发事件、观察患者时的年龄、临床病程中的主要出血表现、疾病的临床严重程度、患者的生存情况以及有助于做出诊断的止血实验室检查。关于出血时间,30例患者出血时间异常,但另外2例患者出血时间正常。