331 top medical experts on Bruton type agammaglobulinemia across 50 countries and 23 U.S. states, including 176 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Bruton type agammaglobulinemia: A clinically variable form of isolated agammaglobulinemia, an inherited immunodeficiency disorder, characterized in affected males by recurrent bacterial infections during infancy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Organizations Providing General Support

  • Synonyms: BTK Agammaglobulinemia,  Bruton tyrosine kinase Agammaglobulinemia,  X-Linked Agammaglobulinemia,  Type I X-Linked Agammaglobulinemia,  Bruton's Agammaglobulinemia,  Bruton-Type Agammaglobulinemia,  Bruton-type (congenital X-linked) agammaglobulinemia,  Congenital Agammaglobulinemia,  Immunodeficiency 1,  X-linked agammaglobulinemia

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