Skip navigation | ||
|
||
Medical Encyclopedia |
|
Other encyclopedia topics: | A-Ag Ah-Ap Aq-Az B-Bk Bl-Bz C-Cg Ch-Co Cp-Cz D-Di Dj-Dz E-Ep Eq-Ez F G H-Hf Hg-Hz I-In Io-Iz J K L-Ln Lo-Lz M-Mf Mg-Mz N O P-Pl Pm-Pz Q R S-Sh Si-Sp Sq-Sz T-Tn To-Tz U V W X Y Z 0-9 |
Contents of this page: | |
|
Alternative Names Return to top
IgA deficiencyDefinition Return to top
Selective deficiency of IgA is the most common immune deficiency disorder. Persons with this disorder have low or absent blood levels of a special protein called immune globulin A.
Causes Return to top
IgA deficiency is inherited, which means it's passed down through families. It may be inherited as an autosomal dominant or autosomal recessive trait. It is found in approximately 1 in 700 individuals of European origin. It is less common in people of other ethnicities.
Symptoms Return to top
Persons with this condition often have chronic diarrhea caused by intestinal infections. There are often frequent ear, sinus, and lung infections.
Other symptoms include mouth infections and unexplained asthma or bronchiectasis.
Exams and Tests Return to top
There may be a family history of IgA deficiency. Tests that may be done include:
Treatment Return to top
No specific treatment is available. Some people gradually develop normal levels of IgA without treatment. Individual infections should be treated with appropriate antibiotics. In some cases, longer courses of antibiotics may be needed to prevent recurring infection.
Autoimmune disease treatment is based on the specific problem.
NOTE: Persons with a complete absence of IgA should not be given gamma globulin. Such treatment may lead to allergies or life-threatening anaphylactic shock.
Outlook (Prognosis) Return to top
Selective IgA deficiency is less harmful than many other immunodeficiency diseases.
Some people with IgA deficiency will recover on their own and begin to produce IgA in larger quantities over a period of years.
Possible Complications Return to top
An autoimmune disorder, such as like rheumatoid arthritis and lupus erythematosus, may develop.
Patients with IgA deficiency may develop antibodies to IgA, and can have severe, even life-threatning reactions to transfusions of blood and blood products. If transfusions are necessary, the blood should ideally come from a donor who is also IgA-deficient.
When to Contact a Medical Professional Return to top
Consider genetic counseling if there is a family history of selective IgA deficiency and you plan to have children.
If you have an IgA deficiency, be sure to mention it to the provider if gamma globulin is suggested as a treatment for any condition.
Prevention Return to top
Genetic counseling may be of value to prospective parents with a family history of selective IgA deficiency.
References Return to top
Hoffman R, Benz EJ, Shattil SS, et al. Hematology: Basic Principles and Practice. 4th ed. Orlando, Fl: Churchill Livingstone; 2005.
Mandell GL, Bennett JE, Dolin R. Principles and Practice of Infectious Diseases. 6th ed. London: Churchill Livingstone; 2005.
Update Date: 7/25/2007 Updated by: Donald Accetta, MD, MPH, President, Allergy & Asthma Care, PC, Taunton, MA. Review provided by VeriMed Healthcare Network.
Home | Health Topics | Drugs & Supplements | Encyclopedia | Dictionary | News | Directories | Other Resources | |
Copyright | Privacy | Accessibility | Quality Guidelines U.S. National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20894 National Institutes of Health | Department of Health & Human Services |
Page last updated: 02 January 2008 |