| hyper-IgE | hyperimmunoglobulinemia E |
|---|---|
| SAHIGES | Staphylococcus aureus hyperimmunoglobulinemia E syndrome |
| hyperimmunoglobulinemia E syndrome |
An autosomal dominant disorder marked by high serum levels of IgE; eczema, mucosal candidiasis, and other cutaneous infections; pulmonary infections; retained primary dentition; scoliosis; and increased frequen
Ãâó:
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|---|---|
| hyperimmunoglobulinemia |
abnormally high levels of immunoglobulins in the serum.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| hyperimmunoglobulinemia D s. |
a periodic fever inherited as an autosomal recessive trait, caused by mutations in the gene for mevalonate kinase and having onset usually before one year of age. It is characterized by attacks of high fever preceded by chills, occurring at intervals of approximately 48 weeks and lasting 46 days, often accompanied by headache, arthritis and arthralgia, erythematous lesions, and hepatosplenomegaly; serum IgD levels are continuously high. Called also Dutch-type periodic fever.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| hyperimmunoglobulinemia E s. |
a primary immunodeficiency disorder characterized by recurrent staphylococcal abscesses of skin, lungs, joints, and other sites, pruritic dermatitis, very high serum IgE levels, normal levels of IgG, IgA, and IgM, blood and sputum eosinophilia, low anamnestic antibody responses to booster immunization, and poor antibody and cell-mediated responses to neoantigens. Called also Buckley's s.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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