Prevalence of Malignancy in Common Variable Immunodeficiency Patients at a Tertiary Care Center
Introduction: Common Variable Immunodeficiency (CVID) is the Primary Immunodeficiency most commonly encountered […]
Antibody Deficiencies
Humoral and cellular immune response to Covid-19 vaccines after primary vaccination with a 3-dose scheme and boosters vaccines in Brazilian patients with Inborn Errors of Immunity compared to healthy controls
Introduction: We investigated humoral and cellular immune responses to Covid-19 vaccines after
SARS-CoV-2 infection in a patient with X-linked agammaglobulinemia: clinical evolution and Covid-19 vaccines responses
Introduction: X-linked agammaglobulinemia (XLA) presents challenges in relation to SARS-CoV-2 infection: prolonged
HELICOBACTER CINAEDI INFECTION ON A FEMALE PATIENT WITH AGAMAGLOBULINEMIA WITH MUTATION IN THE BTK GEN. CASE REPORT
XLA characterized by increased susceptibility to severe hypogammaglobulinemia-related infections. Heterozygous females carry
“Inborn error of selective antibody immunity: IgG3 deficiency”. Case report
Introduction Selective IgG subclass deficiency is one of the 4 most common
“Inborn error of selective antibody immunity: IgG3 deficiency”. Case report Read More »
Hyper-IgM (HIGM) syndrome with uracil -N- glycosylase (UNG) deficiency; First case reported in Mexico.
Hyper-IgM syndrome due to UNG deficiency is a very rare entity with
Ectodermal dysplasia with immunodeficiency when NEMO is not the cause
Ectodermal dysplasias (ED) are genodermatoses sometimes associated with immune deficiency (ED-ID) usually
Ectodermal dysplasia with immunodeficiency when NEMO is not the cause Read More »
ISOLATED IgG3 DEFICIENCY IN ONE ADULT PATIENT WITH AUTOIMMUNE HYPOTHYROIDISM AND LATE ONSET SEVERE ASTHMA: A CASE REPORT.
INTRODUCTION: Deficiency of IgG (one or more IgG subclases) it’s defined as
Phenotypic profile among patients with Autoimmune Cytopenia’s in Common Variable Immunodeficiency
Introduction: Common variable immunodeficiency (CVID) is the most common symptomatic primary immunodeficiency
CASE SERIES: X-LINKED AGAMMAGLOBULINEMIA
INTRODUCTION: Primary immunodeficiencies (PIDs) are a group of diseases caused by genetic
CASE SERIES: X-LINKED AGAMMAGLOBULINEMIA Read More »
