2. Bruton agammaglobulinemia
Bruton agammaglobulinemia is an X-linked genetic condition caused by an abnormality in a key enzyme needed for proper function of the immune system. People who have this disorder have low levels of protective antibodies and are vulnerable to repea...
Healthline.com (OMS Preferred Provider)

3. X-linked agammaglobulinemia - Genetics Home Reference
X-linked agammaglobulinemia (XLA) is a condition that affects the immune system and occurs almost exclusively in males. People with XLA have very few B cells, which are specialized white blood cells that help protect the body against infection. B ...
MedlinePlus (Offsite)

4. X-linked agammaglobulinemia - References - Genetics Home Reference
These sources were used to develop the Genetics Home Reference condition summary on X-linked agammaglobulinemia.
MedlinePlus (Offsite)

5. Agammaglobulinemia
Agammaglobulinemia is an inherited disorder in which there are very low levels of protective immune proteins called immunoglobulins. People with this disorder develop repeated infections.
www.uhseast.com

6. Agammaglobulinemia
Agammaglobulinemia is an inherited disorder in which there are very low levels of protective immune system proteins called immunoglobulins. People with this disorder repeatedly develop infections.
www.clarian.org

7. X-linked Agammaglobulinemia
X-linked agammaglobulinemia, also called Bruton's agammaglobulinemia or congenital agammaglobulinemia, was the first immunodeficiency disease ever identified. "X-linked" means that the gene which causes this agammaglobulinemia...
www.muschealth.com

8. Autosomal Recessive Agammaglobulinemia
Autosomal recessive agammaglobulinemia is a term used to describe a group of inherited disorders of the immune system that affect males and females equally. These disorders are characterized by the onset of recurrent bacterial infections in the fi...
www.stjude.org

9. Bruton Agammaglobulinemia: eMedicine Dermatology
X-linked agammaglobulinemia (XLA), or Bruton agammaglobulinemia, is an inherited immunodeficiency disease caused by mutations in the gene coding for Bruton tyrosine kinase (BTK). The disease was first elucidated by Bruton in 1952, for whom the gen...
emedicine.medscape.com

10. X-linked agammaglobulinemia
The VI International Conference on Rare Diseases and Orphan Drugs (ICORD 2010) for the first time will be convened in the southern hemisphere in agreement with its aim of globalization of rare diseases research and orphan products development acti...
www.rarediseases.info.nih.gov