The CD55 complement inhibitor Eculizumab controls the disease manifestations in a Colombian patient affected with CHAPLE Syndrome
Introduction. Patients with CHAPLE syndrome due to loss-of-function biallelic variants in CD55 […]
Complement Deficiencies
Correlation between D-Dimer levels with the number of attacks of Hereditary Angioedema type 1
Introduction: Hereditary Angioedema is a rare, autosomal dominant disorder characterized by episodes
QUALITY OF LIFE IN HEREDITARY ANGIOEDEMA IN BRAZIL: A MULTICENTRIC STUDY
Introduction: As the medicine evolves quickly and begins to understand the patient
QUALITY OF LIFE IN HEREDITARY ANGIOEDEMA IN BRAZIL: A MULTICENTRIC STUDY Read More »
LIVING WITH HEREDITARY ANGIOEDEMA IN ECUADOR. CASE REPORT ON A PREGNANT PATIENT
INTRODUCTION:Hereditary angioedema is an inborn error of immunity, due to complement deficiency,
LIVING WITH HEREDITARY ANGIOEDEMA IN ECUADOR. CASE REPORT ON A PREGNANT PATIENT Read More »
CASE REPORT OF TYPE 1 HEREDITARY ANGIOEDEMA
INTRODUCTION: Hereditary Angioedema (HA), is an autosomal dominant disease caused by the
CASE REPORT OF TYPE 1 HEREDITARY ANGIOEDEMA Read More »
Diagnosis and treatment of patients with hereditary angioedema in Cuba
Introduction:Hereditary angioedema (HAE) is a primary immunodeficiency with a rare autosomal dominant
Diagnosis and treatment of patients with hereditary angioedema in Cuba Read More »
