Hyper-IgM Syndrome: Introduction
Immunodeficiency with hyper-IgM (HIM) is a rare primary immunodeficiency characterized by the production of normal to increased amounts of IgM antibody of ... more about Hyper-IgM Syndrome.
Hyper-IgM Syndrome: A rare inherited immunodeficiency disorder which causes frequent infections involving the ears, eyes, sinuses, lungs, skin, respiratory tract and other areas of the body.
More detailed information about the symptoms,
causes, and treatments of Hyper-IgM Syndrome is available below.
Symptoms of Hyper-IgM Syndrome
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symptoms of Hyper-IgM Syndrome
Treatments for Hyper-IgM Syndrome
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Wrongly Diagnosed with Hyper-IgM Syndrome?
Hyper-IgM Syndrome: Related Patient Stories
Diagnostic Tests for Hyper-IgM Syndrome
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Hyper-IgM Syndrome: Complications
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Causes of Hyper-IgM Syndrome
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Disease Topics Related To Hyper-IgM Syndrome
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Research about Hyper-IgM Syndrome
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Statistics for Hyper-IgM Syndrome
Hyper-IgM Syndrome: Broader Related Topics
Types of Hyper-IgM Syndrome
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Article Excerpts about Hyper-IgM Syndrome
Genes and Disease by the National Center for Biotechnology (Excerpt)
Immunodeficiency with hyper-IgM (HIM) is a rare primary immunodeficiency characterized by the production of normal to increased amounts of IgM antibody of questionable quality and an inability to produce sufficient quantities of IgG and IgA. Individuals with HIM are susceptible to recurrent bacterial infections and are at an increased risk of autoimmune disorders and cancer at an early age.
(Source: Genes and Disease by the National Center for Biotechnology)
Primary Immune Deficiency, NIAID Fact Sheet: NIAID (Excerpt)
Hyper-IgM is a rare immunodeficiency
disease in which the immune system fails to produce IgA and IgG
antibodies. (Source: excerpt from Primary Immune Deficiency, NIAID Fact Sheet: NIAID)
Definitions of Hyper-IgM Syndrome:
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Hyper-IgM Syndrome as a "rare disease".
Source - Orphanet
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