Diagnosis

Diagnosis involves a medical history of repeat infections and a physical exam. Blood tests and maybe genetic testing can confirm the diagnosis.

Treatment

There's no cure for XLA. Treatment aims at boosting the immune system to prevent infections. There also is quick treatment for infections as they happen.

Medications

Medicines to treat XLA include:

  • Gammaglobulin. This is a type of protein found in blood that contains antibodies against infections. It's put into a vein, called infusion, every 2 to 4 weeks or given with weekly shots.

    Reactions to gammaglobulin can include headache, chills, backache and nausea. Reactions are more likely to happen during a viral infection, such as a cold.

  • Antibiotics. Some people with XLA take antibiotics all the time to prevent infections. Others take antibiotics for bacterial infections longer than do people without XLA.

Your healthcare professional likely will suggest that you have follow-up visits every 6 to 12 months to screen for complications of XLA. You'll also likely be told to not get live vaccines, such as live polio, measles-mumps-rubella or chickenpox vaccines.

Clinical trials

Explore Mayo Clinic studies testing new treatments, interventions and tests as a means to prevent, detect, treat or manage this condition.

Jan. 10, 2024

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  1. X-linked agammaglobulinemia. Genetic and Rare Diseases Information Center. https://rarediseases.info.nih.gov/diseases/1033/x-linked-agammaglobulinemia. Accessed Sept. 28, 2023.
  2. Hernandez-Trujillo VP. Agammaglobulinemia. https://www.uptodate.com/contents/search. Accessed Sept. 28,2023.
  3. X-linked agammaglobulinemia. Merck Manual Professional Version. https://www.merckmanuals.com/professional/immunology-allergic-disorders/immunodeficiency-disorders/x-linked-agammaglobulinemia. Accessed Nov. Sept. 28, 2023.
  4. AskMayoExpert. Common variable immunodeficiency. Mayo Clinic; 2023.
  5. Agammaglobulinemia: X-linked and autosomal recessive. Immune Deficiency Foundation. https://primaryimmune.org/about-primary-immunodeficiencies/specific-disease-types/agammaglobulinemia-x-linked-autosomal-recessive/?gclid=EAIaIQobChMIuPyMwJ2D5gIVyEXVCh2P3AYZEAAYASAAEgJY_fD_BwE. Accessed Nov. 24, 2019.
  6. Brown AY. Allscripts EPSi. Mayo Clinic. Nov.14, 2019.

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