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B cell progenitor kinase (medical condition): Immune deficiency from lack of antibodies.
See also:
X-Linked Agammaglobulinemia:
»Introduction: X-Linked Agammaglobulinemia
»Symptoms of X-Linked Agammaglobulinemia
»Tests for X-Linked Agammaglobulinemia
»Treatments for X-Linked Agammaglobulinemia
These medical condition or symptom topics may be relevant to medical information for B cell progenitor kinase:
B cell progenitor kinase is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that B cell progenitor kinase, or a subtype of B cell progenitor kinase,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
B cell progenitor kinase: Another name for X-Linked Agammaglobulinemia (or close medical condition association).
»Introduction: X-Linked Agammaglobulinemia
»Symptoms of X-Linked Agammaglobulinemia
»Treatments for X-Linked Agammaglobulinemia
B cell progenitor kinase: B cell progenitor kinase is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of B cell progenitor kinase incude:
See full list of 15 symptoms of B cell progenitor kinase (X-Linked Agammaglobulinemia)
Treatments for B cell progenitor kinase (X-Linked Agammaglobulinemia) include:
Read more about treatments for B cell progenitor kinase
Treatment of B cell progenitor kinase: For more treatment information about B cell progenitor kinase, see treatment of X-Linked Agammaglobulinemia (B cell progenitor kinase)
XLA is sometimes called Bruton type, X-linked infantile, or congenital agammaglobulinemia. One out of 100,000 people have XLA. Defects on the X chromosome cause XLA. Only boys get XLA. That is because girls have two sets of X chromosomes, and the normal copy compensates for the faulty gene. (Source: excerpt from Primary Immune Deficiency, NIAID Fact Sheet: NIAID)
These medical disease topics may be related to B cell progenitor kinase:
Source - NIH
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