
The second edition of Primary Immunodeficiency Diseases presents discussions of gene identification, mutation detection, and clinical and research applications for over 100 genetic immune disorders--disorders featuring an increased susceptibility to infections and, in certain conditions, an icreased rate of malignancies and autoimmune disorders. Since the publication of the first edition, a flurry of new disease entities has been defined and new treatment regimens have been introduced, the most spectacular being successful treatment by gene therapy for two genotypes of combined immunodeficiency. The first edition marked a historic turning point in the field of immunodeficiencies, demonstrating that many of the disorders of the immune systam could be understood at a molecular level. This new edition can proudly document the tremendous pace of progress in dissecting the complex immunologic networks responsible for protecting individuals from these disorders.
This text investigates the molecular and cellular mechanisms underlying over 100 distinct genetic immune disorders to provide a comprehensive clinical and research framework. The authors, C. I. Edward Smith, Hans D. Ochs, and Jennifer M. Puck, utilize their extensive expertise in immunology and genetics to synthesize current knowledge on gene identification and mutation detection. The book argues that understanding these conditions at the molecular level is essential for advancing diagnostic accuracy and developing targeted therapeutic interventions, including gene therapy.
What You Will Find
Experts recognize this volume as a foundational reference for clinicians and researchers working within the field of clinical immunology. Readers frequently note the technical density of the prose, which serves as a rigorous resource for those seeking to understand the complex immunologic networks involved in genetic disorders.
Page Count:
776
Publication Date:
2006-01-01
Publisher:
Oxford University Press
ISBN-10:
0199747962
ISBN-13:
9780199747962
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