hyper-IgE syndrome


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hyper-IgE syndrome

Hyperimmunoglobulin E syndrome, see there.
References in periodicals archive ?
Due to history, physical findings, and these initial labs, we suspected Hyper-IgE Syndrome. A calculated HIES score was 63 (>40 required for diagnosis).
(i) Identification of Hyper-IgE Syndrome in patients with characteristic history and clinical features can assist in early diagnosis and help initiate preventive measures for future infections and complications.
Tian et al., "Clinical Manifestations and Genetic Analysis of 17 Patients with Autosomal Dominant Hyper-IgE Syndrome in Mainland China: New Reports and a Literature Review," Journal of Clinical Immunology, vol.
Goel et al., "TH17 Cells in STAT3 Related Hyper-IgE Syndrome," The Indian Journal of Pediatrics, vol.
Holland et al., "Genetic Linkage of Hyper-IgE Syndrome to Chromosome 4," American Journal of Human Genetics, vol.
Binodini, "Autosomal-Recessive Hyper-IgE syndrome," Indian Journal of Dermatology, vol.
Anover-Sombke et al., "Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced TH17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome," The Journal of Allergy and Clinical Immunology, vol.
Strongin et al., "Gastrointestinal Manifestations of STAT3-Deficient Hyper-IgE Syndrome," Journal of Clinical Immunology, vol.
Clinial Use of Immunoglobulin E (IgE) Measurements Measurement of IgE always indicated in patients with suspected IgE monoclonal gammopathy Hyper-IgE syndrome Allergic bronchopulmonary aspergillosis Immunodeficiency syndromes Measurement of IgE sometimes indicated in patients with suspected Allergic disease Helminthic parasitism Measurement of IgE usually not indicated in patients with suspected Inflammatory diseases Nonparasitic infectious diseases