Selective Immunoglobulins deficiency in relatives antibody deficiency patient

Introduction: one of the most common inborn errors of immunity is selective IgA deficiency. Objetive: determine the prevalence of selective IgA deficiency   in first-degree relatives of patients diagnosed with this immunological deficiency included in the registry of inborn errors of immunity in San...

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Main Authors: Yralys Naranjo Herrera, María del Carmen Chávez Alfonso, Valia Concepción Ulloa, Cándido Marcos León Márquez, Grace Alicia De Lara García, Ernesto Gabriel Caraballosa Yero
Format: Article
Language:Spanish
Published: Editorial Ciencias Médicas 2025-02-01
Series:Acta Médica del Centro
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Online Access:https://revactamedicacentro.sld.cu/index.php/amc/article/view/2055
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author Yralys Naranjo Herrera
María del Carmen Chávez Alfonso
Valia Concepción Ulloa
Cándido Marcos León Márquez
Grace Alicia De Lara García
Ernesto Gabriel Caraballosa Yero
author_facet Yralys Naranjo Herrera
María del Carmen Chávez Alfonso
Valia Concepción Ulloa
Cándido Marcos León Márquez
Grace Alicia De Lara García
Ernesto Gabriel Caraballosa Yero
author_sort Yralys Naranjo Herrera
collection DOAJ
description Introduction: one of the most common inborn errors of immunity is selective IgA deficiency. Objetive: determine the prevalence of selective IgA deficiency   in first-degree relatives of patients diagnosed with this immunological deficiency included in the registry of inborn errors of immunity in Sancti Spiritus province until 2023 year. Methods: a cross-sectional descriptive study was carried out in Sancti Spiritus province from July 1st,2020 to December 31st, 2023.The population was made up of 36 first-degree relatives of the 15 patients with selective IgA deficiency diagnosed, included in the Provincial Registry of inborn errors of immunity. The three relatives with serum IgA dosage below normal values for their range of age were respondents. Results: decreased IgA and IgG values were found only in some first-degree relatives and all showed IgM and CD3+CD4+T lymphocyte numbers within normal parameters. Female patients, adults and the mother as a predominated relative, most of them being asymptomatic. Conclusions: In a fifth part of the families with selective IgA deficiency patient studied, new cases with this immunological deficiency appeared. Asymptomatic disease was the most frequent phenotype.
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spelling doaj-art-1eac61fe7db94f45ac28773aaafbcde52025-02-05T02:11:03ZspaEditorial Ciencias MédicasActa Médica del Centro2709-79272025-02-01191e2055e20551286Selective Immunoglobulins deficiency in relatives antibody deficiency patientYralys Naranjo Herrera0María del Carmen Chávez Alfonso1Valia Concepción Ulloa2Cándido Marcos León Márquez3Grace Alicia De Lara García4Ernesto Gabriel Caraballosa Yero5Hospital General Provincial “Camilo Cienfuegos”, Sancti Spíritus, CubaHospital General Provincial “Camilo Cienfuegos”, Sancti Spíritus, CubaHospital General Provincial “Camilo Cienfuegos”, Sancti Spíritus, CubaHospital General Provincial “Camilo Cienfuegos”, Sancti Spíritus, CubaHospital General “Tomas Carrera Galiano”, Trinidad, Sancti Spíritus, CubaHospital General Provincial “Camilo Cienfuegos”, Sancti Spíritus, CubaIntroduction: one of the most common inborn errors of immunity is selective IgA deficiency. Objetive: determine the prevalence of selective IgA deficiency   in first-degree relatives of patients diagnosed with this immunological deficiency included in the registry of inborn errors of immunity in Sancti Spiritus province until 2023 year. Methods: a cross-sectional descriptive study was carried out in Sancti Spiritus province from July 1st,2020 to December 31st, 2023.The population was made up of 36 first-degree relatives of the 15 patients with selective IgA deficiency diagnosed, included in the Provincial Registry of inborn errors of immunity. The three relatives with serum IgA dosage below normal values for their range of age were respondents. Results: decreased IgA and IgG values were found only in some first-degree relatives and all showed IgM and CD3+CD4+T lymphocyte numbers within normal parameters. Female patients, adults and the mother as a predominated relative, most of them being asymptomatic. Conclusions: In a fifth part of the families with selective IgA deficiency patient studied, new cases with this immunological deficiency appeared. Asymptomatic disease was the most frequent phenotype.https://revactamedicacentro.sld.cu/index.php/amc/article/view/2055inmunodeficiencia selectiva de igafamiliares de primer grado
spellingShingle Yralys Naranjo Herrera
María del Carmen Chávez Alfonso
Valia Concepción Ulloa
Cándido Marcos León Márquez
Grace Alicia De Lara García
Ernesto Gabriel Caraballosa Yero
Selective Immunoglobulins deficiency in relatives antibody deficiency patient
Acta Médica del Centro
inmunodeficiencia selectiva de iga
familiares de primer grado
title Selective Immunoglobulins deficiency in relatives antibody deficiency patient
title_full Selective Immunoglobulins deficiency in relatives antibody deficiency patient
title_fullStr Selective Immunoglobulins deficiency in relatives antibody deficiency patient
title_full_unstemmed Selective Immunoglobulins deficiency in relatives antibody deficiency patient
title_short Selective Immunoglobulins deficiency in relatives antibody deficiency patient
title_sort selective immunoglobulins deficiency in relatives antibody deficiency patient
topic inmunodeficiencia selectiva de iga
familiares de primer grado
url https://revactamedicacentro.sld.cu/index.php/amc/article/view/2055
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AT valiaconcepcionulloa selectiveimmunoglobulinsdeficiencyinrelativesantibodydeficiencypatient
AT candidomarcosleonmarquez selectiveimmunoglobulinsdeficiencyinrelativesantibodydeficiencypatient
AT gracealiciadelaragarcia selectiveimmunoglobulinsdeficiencyinrelativesantibodydeficiencypatient
AT ernestogabrielcaraballosayero selectiveimmunoglobulinsdeficiencyinrelativesantibodydeficiencypatient