Primary Immunodeficiency Center in Minnesota

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Diseases

More than 150 distinct types of primary immunodeficiencies have been identified. Among these disorders are:

• Ataxia telangiectasia
• Cartilage hair hypoplasia
• CD40 ligand
• Chediak-Higashi syndrome
• Chronic granulomatous disease
• Chronic mucocutaneous candidiasis
• Common variable immunodeficiency
• Complement deficiencies
• Congenital agranulocytousis (Kostmann syndrome)
• Cyclic neutropenia
• DiGeorge syndrome
• Familial hemophagocytic lymphohistiocytosis (FHL)
• Familial Mediterranean fever (FMF)
• Griscelli syndrome (GS)
• Hereditary angioedema (HAE)
• Hyper IgE syndrome (HIES)
• Hyper IgD syndrome (HIDS)
• Hyper IgM syndromes
• IgG subclass deficiency
• Immunodeficiency with thymoma (Good syndrome)
• Immunodysregulation polyendocrinopathy enteropathy X-linked syndrome (IPEX)
• Interferon-g, interleukin 12, and receptor deficiencies
• Leukocyte adhesion defect (LAD)
• Mannan-binding lectin deficiency (MBL)
• MHC class II deficiency
• Partial combined immunodeficiencies
• Periodic fever aphthous stomatitis, pharyngitis and adenopathy (PFAPA)
• Properdin deficiency
• Severe combined immunodeficiency
• Selective IgA deficiency
• Transient hypoagammaglobulinemia of infancy
• Tumor necrosis factor receptor associated periodic syndrome (TRAPS)
• Wiskott-Aldrich syndrome
• X-linked agammaglobulinemia
• X-linked hyper IgM syndrome
• X-linked lymphoproliferative
• X-linked severe combined immunodeficiency
• X-linked lymphoproliferative syndrome (Duncan syndrome)