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17p11.2 GeneReviews Google OMIM Orphanet PubMed Wikipedia Common variable immunodeficiency *Gene map locus 17p11.2 CVID Common variable hypogammaglobulinemia Hypogammaglobulinemia, acquired Immunoglobulin deficiency, late-onset [Clinical features: hypogammaglobulinemia; antibody deficiency; recurrent bacterial infections] [Inheritance: autosomal recessive; autosomal dominant; isolated cases] |
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Common variable immunodeficiency (CVID) presenting with malabsorption due to giardiasis |
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Turkish Journal of Gastroenterology |
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Edited by Aldo Campana,
March 14, 2010
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