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Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/24208
Title: Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome
Authors: Sanal, Özden
Tezcan, İlhan
Ersoy, Figen
Uludağ Üniversitesi/Tıp Fakültesi/Pediatri Bölümü.
Kılıç, Sara Şebnem
34975059200
Keywords: Bone abnormalities
Hyperimmunoglobulin E syndrome
Osteochondritis dissecans
Osteopenia
Issue Date: 2002
Publisher: Türkiye Milli Pediatri Derneği
Citation: Kılıç, S. S. vd. (2002). "Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome". Turkish Journal of Pediatrics, 44(4), 357-359.
Abstract: Hyperimmunoglobulin E syndrome (hyper-IgE) is a rare immunodeficiency disease associated with recurrent pyogenic infections, chronic eczematoid dermatitis and osteopenia. We present here a 13-year-old girl with hyperimmunoglobulin E syndrome, who developed osteochondritis dissecans (OCD) of the lateral femoral condyle, which is rare. Osteopenia, which is frequently associated with hyper IgE, may predispose the patient to the development of OCD.
URI: http://hdl.handle.net/11452/24208
ISSN: 0041-4301
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Web of Science

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