IMMUNODEFICIENCIES AT AN ADULT IMMUNOLOGY CENTER OVER FOUR DECADES OF FOLLOW UP. AN UPDATE
Introduction Immunodeficiencies (IDs) can be classified as inborn errors of immunity (IEIs) […]
Antibody Deficiencies
Micosis fungoide (Linfoma cutáneo de células T) como manifestación de deficiencia de subclases de IgG en un paciente con dermatitis atópica severa refractaria.
Masculino de 33 años con antecedentes familiares de enfermedad cardiovascular y diabetes,
A previously not reported variant in BTK gene: an atypical late onset case report
Pathogenic variants in BTK gene are associated with X-linked agammaglobulinemia, characterized by
A previously not reported variant in BTK gene: an atypical late onset case report Read More »
X-linked agammaglobulinemia, a case report
Introduction: X-linked agammaglobulinemia (XLA) is an inborn error of immunity, caused by
X-linked agammaglobulinemia, a case report Read More »
“MORBIDITY ASSOCIATED WITH DELAYED DIAGNOSIS IN INBORN ERRORS OF IMMUNITY”
INTRODUCTION: Morbidity is defined as the occurrence of disease, symptoms of disease,
“MORBIDITY ASSOCIATED WITH DELAYED DIAGNOSIS IN INBORN ERRORS OF IMMUNITY” Read More »
Phenotypification on a common variable immunodeficiency population in a third level center
Authors: César Fidel Nogueda García(1), Patricia María O´Farrill Romanillos (1) (1) Instituto
Echocardiographic changes related to pulmonary hypertension in humoral inmunodeficiencies
Introduction Primary humoral immunodeficiencies leads to recurring infections primarily in mucosal surfaces
Defects in ciliary arrangement a simulator of an inborn error of immunity.
Defects in ciliary arrangement a simulator of an inborn error of immunity.
Defects in ciliary arrangement a simulator of an inborn error of immunity. Read More »
Episcleritis as the first clinical manifestation of autoimmunity in patients with common variable immunodeficiency
Female, 10 years old, diagnosed with Inborn Error of Immunity Predominantly Antibodies,
X-linked agammaglobulinemia: sociodemographic and clinicopathological characteristics in a pediatric population.
Introduction: X-linked agammaglobulinemia (XLA) is due to mutations in the BTK gene.
