Job’s syndrome is a rare immunological disorder that displays characteristic dentofacial
features. We present an unusual finding of a post-traumatic upper lip abscess that
was promptly managed by drainage and antimicrobial drugs.
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References
- Hyper IgE (Job’s) syndrome: a primary immune deficiency with oral manifestations.Oral Dis. 2009; 15: 2-7
- The hyper-IgE syndrome.Clin Rev Allergy Immunol. 2001; 20: 139-154
- Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.J Allergy Clin Immunol. 2010; 125: 424-432
- Hyper IgE syndrome associated with novel and recurrent STAT3 mutations: two case reports.Medicine (Baltimore). 2019; 98e14003
- Dental observations of hyper IgE disorder.J Clin Pediatr Dent. 2007; 32: 69-72
Article info
Publication history
Published online: October 24, 2019
Identification
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© 2019 Published by Elsevier Ltd on behalf of The British Association of Oral and Maxillofacial Surgeons.
