A patient with hyper-IgE syndrome: A multisystem disorder - 11/05/12
Doi : 10.1067/mjd.2002.108585
Ralf Hinrichs, MDa, Oliver Fricke, MDb, Rengin Tütüncü, DDSc, Nicolas Hunzelmann, MDa, Thomas Krieg, MDa, Karin Scharffetter-Kochanek, MDa
Cologne, Germany
From the Department of Dermatology,a Center of Pediatric Endocrinology and Metabolism, Children's Hospital,b and Department of Operative Dentistry and Periodontology,c University of Cologne
Abstract |
A patient with hyper-IgE syndrome came to our attention with an exacerbation of atopic dermatitis. The medical evaluation showed typical features of hyper-IgE syndrome and a low number of cytotoxic T cells in the peripheral blood. This case serves as a reminder that hyper-IgE syndrome is a multisystem disorder. (J Am Acad Dermatol 2002;47:S268-9.)
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 | This supplement is made possible through an unrestricted educational grant from Stiefel Laboratories to the American Academy of Dermatology. |
| Reprint requests: Karin Scharffetter-Kochanek, MD, Department of Dermatology, University of Cologne, Joseph-Stelzmann-Str. 9, 50924 Cologne, Germany. E-mail: Karin.Scharffetter@unikoeln.de. |
© 2002
American Academy of Dermatology, Inc. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
Vol 47 - N° 5S
P. S268-S269 - novembre 2002 Ritorno al numero
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