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PedAM

Pediatric Disease Annotations & Medicines




Disease eosinophilia
Phenotype C0022398|hyper-ige syndrome
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PubMedID- 23247359 Multiple deletions and single mutations in zir3 have resulted in an immunodeficiency syndrome,34 and an autosomal-recessive form of hyper-ige syndrome,35,36 presenting with eosinophilia (increased eosinophil count in peripheral blood), increased serum ige levels and recurrent pneumonia, skin abscesses and viral infections.

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