Hyper-IgE recurrent infection syndrome 1, autosomal dominant

A condition of decreased or absent presence or activity of signal transducer and activator of transcription 3 protein. Deficiency of this protein is associated with hyper-IgE syndrome.

Also known as: hyper-IgE recurrent infection syndrome, hyperimmunoglobulin E-recurrent infection syndrome, AD hyperimmunoglobulin E syndrome, AD-HIES, Buckley syndrome, HIES autosomal dominant, HIES, autosomal dominant, JOB syndrome

91 clinical trials for this condition and its sub-types.