Resumen

LEMOS, Felipe; PEDREIRA, Graciela  y  GOMEZ, Rosario. Rare bleeding disorder in a Uruguayan family. Congenital α2-antiplasmin deficiency in two siblings. Anfamed [online]. 2025, vol.12, n.2, e403.  Epub 01-Dic-2025. ISSN 2301-1254.  https://doi.org/10.25184/anfamed2025v12n2a8.

Congenital α2-antiplasmin (α2AP) deficiency is a very rare bleeding disorder caused by impaired fibrinolysis. We present the clinical cases of two brothers with congenital α2AP deficiency.

Palabras clave : Fibrinolysis; α2-antiplasmin; rare bleeding disorder.

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