Deficiencia congénita de factor XI I I . Reporte de un caso (primero en Cuba)
Abstract
Se presenla, por primera vez en Cuba, un caso que se
diagnostica como deficiencia congénita del factor XIII.
Se destacan los elementos de juicio clínico que deben
hacer sospechar el trastorno, insistiendo en la
importancia de la anamnesis remota, y posible
consanguinidad de los padres. Así mismo, se hace
referencia a la significación que tiene esta deficiencia
como favorecedora de abortos espontáneos y los
trastornos que es rapaz de producir en la cicatrización
de las heridas. Se señala lo fundamental del uso del
plasma fresco o congelado para corregir las
manifestaciones de la enfermedad.
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