Immune and Clinical Assessment in a Cohort of Pediatric Hispanic Patients with Partial Digeorge Syndrome: An Institutional Review

Rationale DiGeorge syndrome (DGS) is the result of microdeletions of chromosome 22q11.2, resulting in a highly variable phenotype. Since limited clinical information is available, the purpose of this study was to characterize the immunologic status of a cohort of Hispanic DGS patients.

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Veröffentlicht in:Journal of allergy and clinical immunology 2016-02, Vol.137 (2), p.AB224-AB224
Hauptverfasser: Ale, Hanadys, MD, Olavarrieta, Raquel, MD, Beiro, Zaimat, BS, Blouin, William R., MSN, ARNP, CPNP, Hernandez-Trujillo, Vivian P., MD, FAAAAI, Calderon, Jose G., MD
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container_issue 2
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container_title Journal of allergy and clinical immunology
container_volume 137
creator Ale, Hanadys, MD
Olavarrieta, Raquel, MD
Beiro, Zaimat, BS
Blouin, William R., MSN, ARNP, CPNP
Hernandez-Trujillo, Vivian P., MD, FAAAAI
Calderon, Jose G., MD
description Rationale DiGeorge syndrome (DGS) is the result of microdeletions of chromosome 22q11.2, resulting in a highly variable phenotype. Since limited clinical information is available, the purpose of this study was to characterize the immunologic status of a cohort of Hispanic DGS patients.
doi_str_mv 10.1016/j.jaci.2015.12.864
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source Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Allergy and Immunology
Ear diseases
Hispanic people
Immunoglobulins
Lymphocytes
title Immune and Clinical Assessment in a Cohort of Pediatric Hispanic Patients with Partial Digeorge Syndrome: An Institutional Review
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