Distúrbio hemorrágico raro em uma família uruguaia. Deficiência congênita de α2-antiplasmina em dois irmãos
Resumo
A deficiência congênita de α2-antiplasmina (α2AP) é um distúrbio hemorrágico muito raro causado por fibrinólise prejudicada. Apresentamos os casos clínicos de dois irmãos com deficiência congênita de α2AP
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Referências
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