Epidemiological and clinical features of patients with primary antibody deficiency disorders in the East of Turkey

dc.contributor.authorÖzbey, Mehmet Yavuz
dc.contributor.authorAslan, Mehmet
dc.contributor.authorTopal, Erdem
dc.date.accessioned2021-05-29T09:28:29Z
dc.date.available2021-05-29T09:28:29Z
dc.date.issued2019
dc.departmentİnönü Üniversitesien_US
dc.description.abstractAbstract: Aim: To describe the demographic and clinical features of patients diagnosed with primary antibody deficiency Material and Methods: The medical records of pediatric patients who were diagnosed with primary antibody deficiency were reviewed. Patients were diagnosed with primary antibody deficiency based on the European Society for Immunodeficiencies diagnostic criteria. Result: A total of 60 patients with primary antibody deficiency were identified; 39 patients (65%) were male and median age was 5 (1-18) years of age, while median diagnosis age was 3 (6 mo-14 yr) years. Twenty-one patients (35%) were diagnosed with transient hypogammaglobulinemia of infancy, thirteen (21.7%) with selective Ig A deficiency, five (8.3%) with congenital agammaglobulinemia, five (8.3%) with selective Ig M deficiency, five (8.3%) with unclassified hypogammaglobulinemia, four (6.7%) with Ig G subclass deficiency, two (3.3%) with severe combined immune deficiency, two (3.3%) with common variable immunodeficiency, two (3.3%) with hyper Ig M syndrome, and one patient was diagnosed with pneumococcal vaccine responsiveness, respectively. Eleven patients (18.3%) had consanguinity and six patients (10%) had family history. The most common complaint was frequent respiratory tract infections. Four patients had dermatitis in addition to infection. Three patients had hematopoietic stem cell transplantation and 23 patients (38.3%) received intravenous immunoglobulin treatment. Two patients died during the follow up. Conclusion: Our results indicated that diagnosis is delayed and the patients who are diagnosed with primary antibody deficiency frequently have respiratory tract infections.en_US
dc.identifier.doi10.5455/annalsmedres.2018.12.297en_US
dc.identifier.endpage595en_US
dc.identifier.issn2636-7688
dc.identifier.issue4en_US
dc.identifier.startpage593en_US
dc.identifier.trdizinid316113en_US
dc.identifier.urihttps://doi.org/10.5455/annalsmedres.2018.12.297
dc.identifier.urihttps://hdl.handle.net/11616/41988
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/316113
dc.identifier.volume26en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofAnnals of Medical Researchen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleEpidemiological and clinical features of patients with primary antibody deficiency disorders in the East of Turkeyen_US
dc.typeArticleen_US

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