Search Encyclopedia:    
List of Topics Print This Page
 

Agammaglobulinemia


Definition:

Agammaglobulinemia is disorder passed down through families in which a person has very low levels of protective immune system proteins called immunoglobulins. Immunoglobulins are a type of antibody. Low levels of these antibodies make you more likely to get infections.

Alternative Names:

Bruton's agammaglobulinemia; X-linked agammaglobulinemia

Causes, incidence, and risk factors:

Agammaglobulinemia is a rare disorder that mainly affects males. It is caused by a gene defect that blocks the growth of normal, mature immune cells called B lymphocytes.

As a result, the body makes very little (if any) immunoglobulins in the bloodstream. Immunoglobulins play a major role in the immune response, which protects against illness and infection.

Persons with agammaglobulinemia repeatedly develop infections, especially bacterial infections such as Hemophilus influenzae, pneumococci (Streptococcus pneumoniae), and staphylococci. Common sites of infection include:

  • Gastrointestinal tract
  • Joints
  • Lungs
  • Skin
  • Upper respiratory tract

Agammaglobulinemia is inherited, which means other people in your family may have the condition.

Symptoms:

Symptoms include frequent episodes of:

Infections typically appear in the first 4 years of life.

Other symptoms include:

  • Bronchiectasis (a disease in which the small air sacs in the lungs become damaged and enlarged)
  • Unexplained asthma
Signs and tests:

The disorder is confirmed by laboratory measurement of blood immunoglobulins.

Tests include:

Treatment:

Treatment involves taking steps to reduce the number and severity of infections. You will receive immunoglobulins through a vein (IVIG), which boosts your immune system.

Antibiotics are often needed to treat bacterial infections.

Genetic counseling may be helpful.  
Expectations (prognosis):

Treatment with IVIG has greatly improved the health of those who have agammaglobulinemia.

Without treatment, most severe infections are deadly.

Complications:
Calling your health care provider:

Call for an appointment with your health care provider if:

  • You or your child has experienced frequent infections
  • You have a family history of agammaglobulinemia or another immunodeficiency disorder and you are planning to have children (ask the provider about genetic counseling)
Prevention:

Genetic counseling should be offered to prospective parents with a family history of agammaglobulinemia or other immunodeficiency disorders.

References:

Ballow M. Primary immunodeficiency diseases. In: Goldman L, Schafer AI, eds. Cecil Medicine. 24th ed. Philadelphia, PA: Saunders Elsevier;2011:chap 258.

Morimoto Y. Immunodeficiency overview. Prim Care. 2008;35(1):159-173.


Review Date: 5/26/2012
Reviewed By: David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine. Stuart I. Henochowicz, MD, FACP, Associate Clinical Professor of Medicine, Division of Allergy, Immunology, and Rheumatology, Georgetown University Medical School. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M. Health Solutions, Ebix, Inc.

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. Copyright 2002 A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

   View History
  Agammaglobulinemia

   
   

 

About UPHS   Contact Us   Site Map   Privacy Statement   Legal Disclaimer   Terms of Use

The University of Pennsylvania Health System, Philadelphia, PA 1-800-789-PENN © 2014, The Trustees of the University of Pennsylvania