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dc.contributor.authorSadeghi-Shabestari, M
dc.contributor.authorDousti, S
dc.contributor.authorRezamand, A
dc.contributor.authorHarsini, S
dc.contributor.authorRezaei, N
dc.date.accessioned2018-08-26T08:32:57Z
dc.date.available2018-08-26T08:32:57Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52363
dc.description.abstractNeutropenia is characterized by a decrease in circulating neutrophil counts and consequent infections. The present study was performed to describe the clinical and laboratory findings of patients with congenital neutropenia in northwestern Iran. Medical records of 31 patients with congenital neutropenia out of 280 neutropenic patients who had been referred to Tabriz Children's Hospital during a 3-year-period (2011-2014), were reviewed. Thirty-one cases (17 female and 14 male), with a mean age of 46.21آ±37.92 months, were diagnosed to suffer from congenital neutropenia. The disorders associated with congenital neutropenia were combined immunodeficiency (8 cases), severe congenital neutropenia (6 cases), common variable immunodeficiency (4 cases), severe combined immunodeficiency (2 cases), and metabolic syndrome (1 case). The median age of the onset of disease was 13.16آ±12.48 months. The most common clinical manifestations during the course of illness were otitis media (13 cases), pneumonia (12 cases), recurrent aphthous stomatitis, lymphadenopathy, and gingivitis (11 cases). Four neutropenic patients died because of recurrent infections. Neutropenia may occur in the context of the primary immunodeficiency disorders. Unusual, persistent or severe infections always pose a speculation to search for an underlying immunodeficiency syndrome and neutropenia, so as to avoid further life-threatening complications as a result of any delay in diagnosis. é 2018 Tehran University of Medical Sciences. All rights reserved.
dc.language.isoEnglish
dc.relation.ispartofActa Medica Iranica
dc.subjectimmunoglobulin A
dc.subjectimmunoglobulin E
dc.subjectimmunoglobulin M
dc.subjectacidemia
dc.subjectadult
dc.subjectanemia
dc.subjectantibody production
dc.subjectaphthous stomatitis
dc.subjectArticle
dc.subjectataxia telangiectasia
dc.subjectbone marrow biopsy
dc.subjectcancer chemotherapy
dc.subjectclinical article
dc.subjectcombined immunodeficiency
dc.subjectcommon variable immunodeficiency
dc.subjectdelayed diagnosis
dc.subjectdiarrhea
dc.subjecteosinophilia
dc.subjectfailure to thrive
dc.subjectfemale
dc.subjectflow cytometry
dc.subjectgingivitis
dc.subjectglycogen storage disease
dc.subjecthuman
dc.subjecthyper IgE syndrome
dc.subjectjuvenile rheumatoid arthritis
dc.subjectleukopenia
dc.subjectlymphadenopathy
dc.subjectlymphocytopenia
dc.subjectmale
dc.subjectmedical record
dc.subjectmetabolic disorder
dc.subjectmiddle aged
dc.subjectneutrophil count
dc.subjectotitis media
dc.subjectphagocyte dysfunction
dc.subjectpneumonia
dc.subjectsevere combined immunodeficiency
dc.subjectsevere congenital neutropenia
dc.subjectthrombocytosis
dc.titleA single center survey of patients with congenital neutropenia: Report from northwestern Iran
dc.typeArticle
dc.citation.volume56
dc.citation.issue6
dc.citation.spage372
dc.citation.epage378
dc.citation.indexScopus


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