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Abstract
Common variable immunodeficiency (CVID) is a heterogeneous primary immunodeficiency characterized by defective B-lymphocyte differentiation, defective antibody production, and inflammation-induced organ damage. Etiologies for myositis associated with CVID are often elusive. The following is a case of late-onset multiple acyl-CoA dehydrogenase deficiency (MADD) mimicking myositis in a patient concurrently diagnosed with CVID.
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