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Immune and Clinical Assessment in Pediatric Hispanic Vs. Non-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 scarce information is available regarding possible racial differences, the purpose of this study was to characterize the immunologic status of a cohort of Hispanic...

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Bibliographic Details
Published in:Journal of allergy and clinical immunology 2017-02, Vol.139 (2), p.AB21-AB21
Main Authors: Ale, Hanadys, MD, Calderon, Jose G., MD, Beiro, Zaimat, BS, Hernandez-Trujillo, Vivian P., MD, FAAAAI
Format: Article
Language:English
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Summary:Rationale DiGeorge syndrome (DGS) is the result of microdeletions of chromosome 22q11.2, resulting in a highly variable phenotype. Since scarce information is available regarding possible racial differences, the purpose of this study was to characterize the immunologic status of a cohort of Hispanic vs.
ISSN:0091-6749
1097-6825
DOI:10.1016/j.jaci.2016.12.022