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Introduction on Primary Immunodeficiency Diseases
Pages 1-81
The number of diagnosed cases of primary immunodeficiency diseases (PIDs) – a group of inborn disorders of the immune system – is growing rapidly, but misdiagnosis or late diagnosis still occurs in a significant number of patients, with serious consequences. This is the second edition of a practical reference textbook on PIDs that has been widely welcomed by scientists and clinicians from around the world. The new edition has been extensively revised to reflect advances in knowledge and includes various PIDs not previously covered. For each disease, information is provided on definition, etiology, clinical manifestations, diagnosis, and management. This book will represent an ideal resource for specialists when engaging in diagnosis, clinical decision-making, and treatment planning. It will also prove invaluable for doctors in training and other physicians and nurses who wish to learn more about PIDs.
Introduction on Primary Immunodeficiency Diseases
Pages 1-81
Combined T- and B-Cell Immunodeficiencies
Pages 83-182
Predominantly Antibody Deficiencies
Pages 183-244
Phagocytes Defects
Pages 245-294
Genetic Disorders of Immune Regulation
Pages 295-338
Defects in Intrinsic and Innate Immunity: Receptors and Signaling Components
Pages 339-392
Autoinflammatory Disorders
Pages 393-435
Complement Deficiencies
Pages 437-460
Other Well-Defined Immunodeficiencies
Pages 461-517
Syndromic Immunodeficiencies
Pages 519-551
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