Primary Immunodeficiency
American College of Allergy, Asthma, and Immunology, American Academy of Allergy, Asthma & ImmunologyPublished: February 16, 2016
- Key Points
- General Diagnostic Considerations
- Treatment Recommendations
- Combined B- and T-Cell Immunodeficiencies
- Well-Defined Syndromes with Immunodeficiency
- Predominantly Antibody Deficiencies
- Diseases of Immune Dysregulation
- Phagocytic Cell Defects
- Defects of Innate Immunity
- Autoinflammatory Disorders
- Complement Deficiencies & Anti-Cytokine Autoantibodies
- Figures
- General Approach for the Diagnosis of Primary Immunodeficiency
- Diagnosis of Combined or Syndromic Immunodeficiencies
- Diagnosis of Diseases of Immune Dysregulation
- Diagnosis of Phagocyte Defects
- Diagnosis of Innate Immune Defects
- Diagnosis of Autoinflammatory Syndromes
- Tables
- Characteristic Clinical Presentations of Some Immunodeficiency Disorders
- Laboratory Tests of Immune Function
- Summary of Laboratory Findings in the Diagnosis of Antibody Deficiencies
- Summary of Therapeutic Considerations for Primary Immunodeficiencies and their Complications
- Regimens for Prophylaxis of Bacterial Respiratory Tract Infections
- Clinical and Laboratory Manifestations of Selected Combined Immunodeficiencies and Syndromes
- Lymphocyte Phenotype Classification of SCID
- Assessing Serotype-specific Responses to Pneumococcal Capsular Polysaccharides
- Summary of Screening Laboratory Findings and Diagnosis of Complement Deficiencies
- Clinical Associations with Complement Deficiency
- Classification of Primary Immunodeficiencies
- Categories of PIDD
- Internet Resources for PIDDs
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