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Rare association of hyper IgE syndrome with cervical rib and natal teeth
Indian Journal of Dermatology, 11/25/09
Roshan AS et al. – Hyper IgE syndrome (HIES) is a rare immunodeficiency syndrome characterized by a triad of cutaneous abscesses, mostly caused by Staphylococus aureus; pneumonia; and raised IgE levels. Nonimmunological associations include course facial features, multiple bone fractures, joint hyperextensibility, and retained primary dentition. Patients require long–term antibiotic therapy.
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