Publication details

Hyper IgE syndrom - další z primárních imunodeficitů, u něhož byla poznána genetická podstata

Title in English Hyper IgE syndrome - another primary immunodeficiency with resolved genetic cause
Authors

LITZMAN Jiří

Year of publication 2008
Type Article in Periodical
Magazine / Source Alergie
MU Faculty or unit

Faculty of Medicine

Citation
Field Immunology
Keywords primary immunodeficiency; hyper IgE syndrome; STAT3
Description Hyper-IgE syndrome is a complex multisystem disease affecting predominantly immune and musculoskeletal systems, also dental abnormalities are frequent. Immune system disturbances manifest by dermatitis resembling atopic eczema, and recurrent and severe infections affecting skin and respiratory system. Musculoskeletal abnormalities include abnormal face with coarse appearance, pathological fractures, joint hyperextensibility and scoliosis. High serum IgE levels and eosinophilia comprise typical laboratory signs. STAT3 mutations were recently recognized as a genetic cause of the disease.

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