X-Linked Agammaglobulinemia - Research Article from World of Genetics

This encyclopedia article consists of approximately 2 pages of information about X-Linked Agammaglobulinemia.

X-Linked Agammaglobulinemia - Research Article from World of Genetics

This encyclopedia article consists of approximately 2 pages of information about X-Linked Agammaglobulinemia.
This section contains 595 words
(approx. 2 pages at 300 words per page)
Buy the X-Linked Agammaglobulinemia Encyclopedia Article

X-linked agammaglobulinemia (XLA) or Bruton's agammaglobulinemia is present at birth (congenital) and is characterized by low or completely absent levels of immunoglobulins in the bloodstream. Immunoglobulins are protein molecules in blood serum that function like antibodies. Without them, the body lacks a fully functioning immune system. Persons with XLA are vulnerable to repeated, potentially fatal bacterial infections.

XLA occurs in 1 in 50,000 to 1 in 100,000 newborns. Almost all persons with the disorder are males. Although persons with XLA carry the genes to produce immunoglobulins, a genetic defect on the X chromosome prevents their formation. This defect is not associated with the immunoglobulins themselves, but rather with the B cells in the bloodstream that ordinarily secrete the immunoglobulins.

B cells are a type of white blood cell. They are the sole producers of immunoglobulins in the body. B cells are produced in the bone marrow and carried to the...

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This section contains 595 words
(approx. 2 pages at 300 words per page)
Buy the X-Linked Agammaglobulinemia Encyclopedia Article
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