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

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
Format: Artikel
Sprache:eng
Schlagworte:
Allergy and Immunology
Ear diseases
Hispanic people
Immunoglobulins
Lymphocytes
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Zusammenfassung: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.
ISSN:0091-6749
1097-6825
DOI:10.1016/j.jaci.2015.12.864