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This interrupted case study follows the declining health of an infant who suffers from recurrent infections and finally is diagnosed with severe combined immunodeficiency (SCID). The case was developed for use in an undergraduate upper-level immunology course to supplement discussion of B and T cell development and the generation of antibody diversity. It could also be modified for use in a genetics class, with emphasis on the molecular aspects of RAG-mediated recombination and inheritance patterns of the disease, or a pathophysiology class, with emphasis on the physiology underlying the symptoms.
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