INMUNODEFICIENCIA COMBINADA SEVERA: REPORTE DE UN CASO
INTRODUCCION: LA INMUNODEFICIENCIA COMBINADA GRAVE ES UN ERROR INNATO DE LA INMUNIDAD […]
INMUNODEFICIENCIA COMBINADA SEVERA: REPORTE DE UN CASO Read More »
Combined Immunodeficiencies
Two cases of Inborn errors of immunity in a Mennonite population in Chihuahua.
Introduction: Inborn errors of immunity (IEI), have demonstrated a higher prevalence among
Two cases of Inborn errors of immunity in a Mennonite population in Chihuahua. Read More »
Two cases of severe combined immunodeciency caused by Adenosine deaminase deficiency.
Introduction: Adenosine deaminase (ADA) deficiency is a common form of severe combined
Two cases of severe combined immunodeciency caused by Adenosine deaminase deficiency. Read More »
Clinical and immunologic characteristics of patients with clinical and molecular diagnosis of inborn error of immunity.
Introduction: Inborn errors of immunity (IBD) (formerly called primary immunodeficiencies), are rare
Recommendations from the ClinGen SCID VCEP: Implementation of ACMG/AMP Variant Curation Guidelines for Severe Combined Immunodeficiency Disease
The Clinical Genome Resource (ClinGen) is a National Institutes of Health (NIH)-funded
Combined Inmunodeficiency T-B-NK- and BCGosis: Clinical Case
Introduction: Bacille Calmette-Guérin (BCG) is the only live attenuated vaccine to protect
Combined Inmunodeficiency T-B-NK- and BCGosis: Clinical Case Read More »
UNA INMUNODEFICIENCIA COMBINADA GRAVE, SÍNDROME DE OMENN.
Introducción: El síndrome de Omenn es un síndrome de inmunodeficiencia combinada grave
UNA INMUNODEFICIENCIA COMBINADA GRAVE, SÍNDROME DE OMENN. Read More »
When the Child was Not Actin´Out: A Case Report of Inherited Actin-Related Protein 2/3 Complex Subunit 1B Deficiency
ARPC1B deficiency is a recently described rare genetic inborn error of immunity,
A Novel Homozygous Variant in JAK3 in a Patient with Severe Combined Immunodeficiency (SCID) with T-B+NK- Phenotype and Persistent Covid-19.
Introduction: Severe combined immunodeficiency (SCID) is a condition in which defects in
X-linked severe combined immunodeficiency by IL2RG mutation in a Mexican infant.
Introduction: Severe combined immunodeficiency (SCID) refers to a heterogeneous group of disorders
X-linked severe combined immunodeficiency by IL2RG mutation in a Mexican infant. Read More »
