STAT3 mutation in a child with hyper-IgE syndrome and incomplete clinical features
Szaflarska, A.; Rutkowska-Zapała, M.; Pituch-Noworolska, A.; Siedlar, M.
Przeglad Lekarski 72(12): 787-790
2015
ISSN/ISBN: 0033-2240 PMID: 27024962 Document Number: 681095
We described mutation of STAT3 gene, typical for autosomal dominant hiperimmunoglobulin E syndrome (HIES), in a child with recurrent skin abscesses and respiratory tract infections without skeletal and connective tissue anomalies.
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