Forma hereditaria de angioedema causada por disminución de los niveles o de la función del inhibidor de C1 o por otros mecanismos, incluyendo mutaciones de los genes que codifican el factor de coagulación XII, angiopoyetina-1, plasminógeno y otros factores aún indeterminados.
Forma hereditaria de angioedema causada por niveles o función disminuidos de inhibidor de C1 o por otros mecanismos que conducen al aumento de los niveles de bradicinina.
Inherited form of angioedema caused by decreased levels or function of C1 inhibitor or other mechanisms including mutations of the genes encoding coagulation factor XII, angiopoietin-1, plasminogen and as yet undefined factors.
Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain.
Hereditary angioedema (HAE) is a genetic disease characterised by the occurrence of transitory and recurrent subcutaneous and/or submucosal oedemas resulting in swelling and/or abdominal pain.