Open Access
Med Buccale Chir Buccale
Volume 21, Number 2, avril 2015
Page(s) 105 - 108
Section Cas clinique et revue de littérature / Up-to date Review and Case Report
Published online 20 April 2015
  1. Davis SD, Schaller J, Wedgwood RJ. Job’s syndrome: recurrent, “cold”, staphylococcal abscesses. Lancet 1966;1(7445):1013-5. [CrossRef] [Google Scholar]
  2. DeWitt CA, Bishop AB, Buecher LS, Stone SP. Hyperimmunoglobulin E syndrome: two cases and a review of literature. J Am Acad Dermatol 2006;54(5):855-65. [CrossRef] [PubMed] [Google Scholar]
  3. Grimbacher B, Holland SM, Gallin JI, Greenberg F, Hill SC, Malech HL. Hyper-IgE syndrome with recurrent infections - An autosomal dominant multisystem disorder. N Engl J Med 1999;340(9):692-702. [CrossRef] [PubMed] [Google Scholar]
  4. Buckley RH. The hyper IgE syndrome. Clin Rev Allergy Immunol 2001;20(1):139-54. [CrossRef] [PubMed] [Google Scholar]
  5. Van Scoy RE, Hill HR, Ritts RE, Quie PG Familial neutrophil chemotaxis defect, recurrent bacterial infections, mucocutaneous candidiasis, and hyperimmunoglobulinemia E. Ann Intern Med 1975; 82(6):766-71. [CrossRef] [PubMed] [Google Scholar]
  6. Blum R, Geller G, Fish LA. Recurrent severe staphylococcal infections, eczematoid rash, extreme elevations of IgE, eosinophilia, and divergent chemotactic responses in two generations. J Pediatr 1977;90(4):607-9. [CrossRef] [PubMed] [Google Scholar]
  7. L’Huillier JP, Thoreux PH, Delaval P, Desrues B, Le Gall E, Kernec J, et al. The hyperimmunoglobulinaemia E and recurrent infections syndrome in an adult. Thorax 1990;45(9):707-8. [CrossRef] [PubMed] [Google Scholar]
  8. Chamlin SL, McCalmont TH, Cunningham BB, Esterly NB, Lai CH, Mallory SB, et al. Cutaneous manifestations of hyper-IgE syndrome in infants and children. J Pediatr 2002;141(4):572-5. [CrossRef] [PubMed] [Google Scholar]
  9. Borges WG, Hensley T, Carey JC, Petrak BA, Hill HR. The face of Job. J Pediatr 1998;133(2):303-5. [CrossRef] [PubMed] [Google Scholar]
  10. O’Connell AC, Puck JM, Grimbacher B, Facchetti F, Morjana A, Gallin JI, et al. Delayed eruption of permanent teeth in hyperimmunoglobulinemia E recurrent infection syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2000;89(2):177-85. [CrossRef] [PubMed] [Google Scholar]
  11. Domingo DL, Freeman AF, Davis J, Puck JM, Tianxia W, Holland SM, et al. Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome. Oral Dis 2008;14(1):73-81. [PubMed] [Google Scholar]
  12. Freeman AF, Domingo DL, Holland SM. Hyper IgE (Job’s) syndrome: a primary immune deficiency with oral manifestations. Oral Dis 2009;15(1):2-7. [CrossRef] [PubMed] [Google Scholar]
  13. Avery DT, Ma CS, Bryant VL, Santner-Nanan B, Nanan R, Wong M, et al. STAT3 is required for IL-21-induced secretion of IgE from human naive B cells. Blood 2008:1;112(5):1784-93. [CrossRef] [PubMed] [Google Scholar]
  14. Conti HR, Baker O, Freeman AF, Jang WS, Holland SM, Li RA, et al. New mechanism of oral immunity to mucosal candidiasis in hyper-IgE syndrome. Mucosal Immunol 2011;4(4):448-55. [CrossRef] [PubMed] [Google Scholar]
  15. Sepet E, Ozdemir D, Aksakalli N, Külekçig G. Hyper-IgE syndrome: a case report. J Clin Pediatr Dent 2001;25(4):333-6. [CrossRef] [PubMed] [Google Scholar]
  16. Kamasaki Y, Hidaka K, Nishiguchi M, Fujiwara T. Dental manifestations of a pediatric patient with hyperimmunoglobulin E syndrome: a case report. J Dent Child (Chic) 2012;79(2):100-4. [PubMed] [Google Scholar]

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