Chapter 6: IgG Subclass Deficiency and Specific Antibody Deficiency
Download this chapter from the IDF Patient & Family Handbook for Primary Immunodeficiency Diseases, Sixth Edition.
Chapter 5: Hyper IgM Syndromes
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Chapter 4: Selective Immunoglobulin Deficiency: IgA and IgM
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Chapter 3: Common Variable Immune Deficiency Phenotypes
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Chapter 2: Antibody Deficiency with Absent B Cells
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Chapter 1: The Immune System and Primary Immunodeficiency Diseases
Download this chapter from the IDF Patient & Family Handbook for Primary Immunodeficiency Diseases, Sixth Edition.
IDF Patient & Family Handbook for Primary Immunodeficiency
The sixth edition of IDF's handbook contains comprehensive information about the diagnosis, treatment, and management of primary immunodeficiencies.
Wiskott-Aldrich syndrome (WAS)
Wiskott-Aldrich syndrome (WAS) is a rare primary immunodeficiency (PI) that causes bleeding problems and eczema in addition to susceptibility to infections. It is inherited in an X-linked recessive manner.
WHIM syndrome
Warts, hypogammaglobulinemia, immunodeficiency, myelokathexis (WHIM) syndrome is an ultra-rare and difficult-to-diagnose primary immunodeficiency (PI) in which individuals are susceptible to life-threatening bacterial infections and to human papillomavirus (HPV) infections.
Transient hypogammaglobulinemia infancy
When it takes longer than expected for a baby to make their own IgG antibodies, they may have transient hypogammaglobulinemia of infancy (THI).
