Abstract
Common variable immunodeficiency (CVID) is a major antibody-deficiency syndrome, associated with increased risk of bacterial infection, as well as autoimmune and granulomatous disease. The clinical and immunological features are heterogeneous. This heterogeneity is expressed by the case reports of three selected patients. These observations will be discussed, with reference to a recent classification of CVID distinguishing four different clinical entities: i) CVID presenting with clinical and immunological features of X-linked agammaglobulinemia; ii) CVID presenting with clinical and immunological features of X-linked hyper-IgM syndrome; iii) CVID associated with systemic granulomatous disease; and iiii) CVID associated with autoimmune manifestations.
MeSH terms
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Adult
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Agammaglobulinaemia Tyrosine Kinase
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Amino Acid Substitution / genetics
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Autoimmune Diseases / diagnosis
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Autoimmune Diseases / genetics
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Autoimmune Diseases / immunology
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Bacterial Infections / diagnosis
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Bacterial Infections / genetics
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Bacterial Infections / immunology
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Common Variable Immunodeficiency / classification
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Common Variable Immunodeficiency / diagnosis*
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Common Variable Immunodeficiency / genetics
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Common Variable Immunodeficiency / immunology
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DNA Mutational Analysis
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Diagnosis, Differential
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Gastroenteritis / diagnosis
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Gastroenteritis / genetics
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Gastroenteritis / immunology
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Genetic Predisposition to Disease / genetics
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Humans
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Immunization, Passive
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Male
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Middle Aged
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Opportunistic Infections / diagnosis
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Opportunistic Infections / genetics
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Opportunistic Infections / immunology
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Protein-Tyrosine Kinases / genetics
Substances
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Protein-Tyrosine Kinases
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Agammaglobulinaemia Tyrosine Kinase