Autosomal dominant hyperimmunoglobulin E syndrome (Q94318): Difference between revisions
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Síndrome de hiper-IgE autossômica dominante (AD-HIES) é um transtorno de imunodeficiência primária muito raro caracterizado pela tríade clínica de IgE sérica elevada (> 2.000 UI/ml), abscessos cutâneos estafilocócicos recorrentes e pneumonia recorrente com formação de pneumatoceles. | |||
| description / en | description / en | ||
Autosomal dominant hyper-IgE syndrome (AD-HIES) is a very rare primary immunodeficiency disorder characterised by the clinical triad of high serum IgE (>2000 IU/ml), recurring staphylococcal skin abscesses, and recurrent pneumonia with formation of pneumatoceles. | |||
Revision as of 09:27, 16 August 2026
Autosomal dominant hyper-IgE syndrome (AD-HIES) is a very rare primary immunodeficiency disorder characterised by the clinical triad of high serum IgE (>2000 IU/ml), recurring staphylococcal skin abscesses, and recurrent pneumonia with formation of pneumatoceles.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1561846514 |
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| English | Autosomal dominant hyperimmunoglobulin E syndrome |
Autosomal dominant hyper-IgE syndrome (AD-HIES) is a very rare primary immunodeficiency disorder characterised by the clinical triad of high serum IgE (>2000 IU/ml), recurring staphylococcal skin abscesses, and recurrent pneumonia with formation of pneumatoceles. |
