Migratory pneumonia caused by common variable immunodeficiency disorder

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Bronchiectasis caused by common variable immunodeficiency

Primary immunodeficiencies (PIDs) are characterized by impairment of one or more arms of the immune response, resulting in decreased defense, an increased number of infections, and, in certain cases, a higher incidence of autoimmune diseases and cancers.(1) Although PIDs are considered rare diseases, many of them are more common than are those currently diagnosed with the “heel prick” test. The...

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Pneumonia in common variable immunodeficiency after change in environment

Background Common Variable Immunodeficiency (CVID) is a Primary Immunodeficiency characterized by an association of IgG deficiency with IgA and/or IgM deficiency, and a decrease in the function of specific antibodies, discarding other causes of hipogamaglobulinemia. The recurrent pneumonia are among the main clinical manifestations of CVID,which appear between 20 and 40 years of age in most cas...

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Comparison of Diagnostic Criteria for Common Variable Immunodeficiency Disorder

Common variable immunodeficiency disorders (CVIDs) are the most frequent symptomatic primary immune deficiency condition in adults. The genetic basis for the condition is not known and no single clinical feature or laboratory test can establish the diagnosis; it has been a diagnosis of exclusion. In areas of uncertainty, diagnostic criteria can provide valuable clinical information. Here, we co...

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Common variable immunodeficiency.

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Common variable immunodeficiency.

Common variable immunodeficiency (CVID) is a form of severe antibody deficiency with an estimated prevalence of 1 in 25,000 to 1 in 100,000. The disorder apparently results from currently undefined immune deregulations resulting in failed B-cell differentiation with impaired secretion of immunoglobulins. A 5-year female presented with fever, cough and shortness of breath at rest. Past medical h...

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ژورنال

عنوان ژورنال: Egyptian Journal of Chest Diseases and Tuberculosis

سال: 2015

ISSN: 0422-7638

DOI: 10.1016/j.ejcdt.2014.12.006