eMedicine Specialties > Allergy and Immunology > Immunodeficiencies
Immunoglobulin M Deficiency: Follow-up
Updated: Jul 21, 2009
Follow-up
Further Outpatient Care
- Determination of quantitative immunoglobulins (IgM, IgG, IgA, IgE) and IgG subclasses should be performed at periodic intervals (ie, every 1-2 y).
Complications
- Prompt treatment of infections helps to decrease morbidity and mortality.
Prognosis
- Patients with severe life-threatening infections clearly have poor prognoses. Other patients who are asymptomatic may have excellent prognoses.
Patient Education
- Educate patients to promptly report any symptoms of infection.
Miscellaneous
Medicolegal Pitfalls
- Patients should be promptly referred to a clinical immunologist. Quantitative measurements of other immunoglobulin isotypes (in order to exclude other humoral immunodeficiencies) upon discovering low IgM levels must also be done, and the possibility of clonal B-cell disorders should be ruled out.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author Christina O'Relley Barnes, MD, to the development and writing of this article.
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| References |
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References
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Further Reading
Keywords
immunoglobulin M deficiency, IgM deficient, selective IgM deficiency, SIgMD, hypogammaglobulinemia, IgM, IgM deficiency, DiGeorge syndrome, hypocomplementemia, hypogammaglobulinemia, IgA deficiency, IgG deficiency, Wiskott-Aldich syndrome, IgG reference range, Ig reference ranges, common variable immunodeficiency
Follow-up: Immunoglobulin M Deficiency