- any
immunoglobulin infusions needed. The
following lists types of "
agammaglobulinemia"
catalogued in the OMIM.
Hypogammaglobulinemia can have
other types;...
- X-linked
agammaglobulinemia (XLA) is a rare
genetic disorder discovered in 1952 that
affects the body's
ability to
fight infection. As the form of agammaglobulinemia...
-
implicated in the
primary immunodeficiency disease X-linked
agammaglobulinemia (Bruton's
agammaglobulinemia);
sometimes abbreviated to XLA and
selective IgM deficiency...
-
presentations including repeated mild
respiratory infections, and/or
agammaglobulinemia (lack of all or most
antibody production)
which results in frequent...
-
globulins naturally because of an
immune deficiency, such as X-linked
agammaglobulinemia and
hyper IgM syndrome. Such
injections are less
common in modern...
- Cross, H. E. (1966-02-28). "Ataxia-telangiectasia and Swiss-type
agammaglobulinemia. Two
genetic disorders of the
immune mechanism in
related Amish sibships"...
-
cancer and
breast cancer. Some
immune deficiencies, such as X-linked
agammaglobulinemia and hypogammaglobulinemia,
result in
partial or
complete lack of antibodies...
-
condition he
discovered is
sometimes referenced by his name: "Bruton-type
agammaglobulinemia". The gene ****ociated with this
defect is also
named after him: Btk...
- and
gastrointestinal infections. X-linked
agammaglobulinemia (XLA; also
known as
Bruton type
agammaglobulinemia):
characterized by a
deficiency in tyrosine...
-
variable immunodeficiency,
severe combined immunodeficiency, X-linked
agammaglobulinemia, Wiskott–Aldrich syndrome,
DiGeorge syndrome, ataxia–telangiectasia...
