RESUMEN

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.

Asunto(s)

Trastornos de la Coagulación Sanguínea/genética , Adolescente , Adulto , Trastornos de la Coagulación Sanguínea/sangre , Trastornos de la Coagulación Sanguínea/diagnóstico , Trastornos de la Coagulación Sanguínea/terapia , Trastornos de las Plaquetas Sanguíneas/diagnóstico , Niño , Preescolar , Consanguinidad , Diagnóstico Diferencial , Factor VIII/análisis , Femenino , Hemostasis , Humanos , Masculino , Pronóstico , Púrpura Trombocitopénica/diagnóstico , Enfermedades de von Willebrand/diagnóstico