El angioedema hereditario es un padecimiento poco frecuente causado por defectos en el gen del inhibidor del C1, caracterizado típicamente por episodios recurrentes de edema en diferentes regiones del cuerpo, que en algunos casos incluyen edema laríngeo. Las concentraciones séricas bajas del inhibidor del C1 confirman el diagnóstico. ABSTRACT Hereditary angioedema is an uncommon disorder mainly caused by defects of the gene for C1 inhibitor. These patients present recurrent edema episodes in the different regions of the body, including larynx edema in some cases. Low plasma levels of C1 inhibitor confirm the diagnosis
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...
Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and up...
Angioedema is a recurrent, non-pitting, non-pruritic, self-limiting swelling due to transient increa...
El angioedema hereditario o edema angioneurótico familiar (HAE) , es una enfermedad genética rara, d...
C1-inhibitor deficiency can be inherited or acquired; both conditions lead to recurrent angioedema t...
El angioedema hereditario es una enfermedad genética rara, autosómica dominante, con una aparición d...
Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple ...
A new type of hereditary angioedema was described recently. It was characterized by recurrent bouts ...
International audienceAcquired angioedema with C1-inhibitor deficiency is a rare and peculiar entity...
El angiodema hereditario es una enfermedad autosómica dominante, originada por deficiencia del inhib...
Background: Acquired angioedema due to C1-inhibitor deficiency (C1-INH-AAE) is a rare disease with n...
Angioedema due to the acquired deficiency of C1-inhibitor is a rare disease known as acquired angioe...
In this article, three cases of hereditary angioedema (HAE) type III (estrogen-dependent or with nor...
ABSTRACTBackgroundHereditary angioedema (HAE) is a rare but life-threatening condition that results ...
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...
Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and up...
Angioedema is a recurrent, non-pitting, non-pruritic, self-limiting swelling due to transient increa...
El angioedema hereditario o edema angioneurótico familiar (HAE) , es una enfermedad genética rara, d...
C1-inhibitor deficiency can be inherited or acquired; both conditions lead to recurrent angioedema t...
El angioedema hereditario es una enfermedad genética rara, autosómica dominante, con una aparición d...
Hereditary angioedema is an autosomal dominant disease characterized by edema attacks with multiple ...
A new type of hereditary angioedema was described recently. It was characterized by recurrent bouts ...
International audienceAcquired angioedema with C1-inhibitor deficiency is a rare and peculiar entity...
El angiodema hereditario es una enfermedad autosómica dominante, originada por deficiencia del inhib...
Background: Acquired angioedema due to C1-inhibitor deficiency (C1-INH-AAE) is a rare disease with n...
Angioedema due to the acquired deficiency of C1-inhibitor is a rare disease known as acquired angioe...
In this article, three cases of hereditary angioedema (HAE) type III (estrogen-dependent or with nor...
ABSTRACTBackgroundHereditary angioedema (HAE) is a rare but life-threatening condition that results ...
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
Hereditary angioedema (HAE) caused by a deficiency of C1 esterase inhibitor enzyme (C1-INH) is a ver...
Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) causes swelling in the skin and up...