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 »
Case report
RECURRENT SEPTIC ARTHRITIS AS AN INITIAL PRESENTATION OF BRUTON’S AGAMMAGLOBULINEMIA
INTRODUCTION. X-linked agammaglobulinemia is an inborn error of immunity characterized by virtually
RECURRENT SEPTIC ARTHRITIS AS AN INITIAL PRESENTATION OF BRUTON’S AGAMMAGLOBULINEMIA Read More »
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
“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 »
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 »
Incomplete Kawasaki disease versus Multisystem inflammatory syndrome in children as initial manifestation of Blau Syndrome
Introduction Blau Syndrome is an autoinflammatory disorder considered a human inborn error
ATAXIA TELANGIECTASIA: REPORT OF TWO FAMILY CASES.
Ataxia telangiectasia (AT) is a rare combined immunodeficiency syndrome with multisystem involvement,
ATAXIA TELANGIECTASIA: REPORT OF TWO FAMILY CASES. Read More »
A case report of Omenn’s Syndrome in Hospital Infantil de Tlaxcala
Introduction: Omenn syndrome (OS) is characterized by severe combined immunodeficiency (SCID) associated
A case report of Omenn’s Syndrome in Hospital Infantil de Tlaxcala Read More »
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
