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Type: Journal article
Title: Binder syndrome
Author: Chummun, S.
McLean, N.
Nugent, M.
Anderson, P.
David, D.
Citation: Journal of Craniofacial Surgery, 2012; 23(4):986-990
Publisher: Lippincott, Williams & Wilkins
Issue Date: 2012
ISSN: 1049-2275
Statement of
Shaheel Chummun, N.R. McLean, M. Nugent, P. J. Anderson and David J. David
Abstract: Patients with chondrodysplasia punctata (CDP) usually present with Binder-type features, and often CDP is misdiagnosed as Binder syndrome. This study reviewed the management and outcome of patients with Binder syndrome and CDP in a multidisciplinary setting. METHODS: The notes and radiographs of the patients managed at the Australian Craniofacial Unit with a multidisciplinary setting since 1976 were reviewed, and data were collected on patient demographics, associated medical and surgical problems, subsequent management, and complications. RESULTS: Seventy-seven patients were treated over the 30-year period (5 patients were lost to follow-up); of the remaining 72 patients, 60 (83%) had Binder syndrome, and 12 (17%) were patients with CDP. Forty were males, and 32 were females, with an age range of 6 months to 47 years. Thirteen patients (18%) had a strong family history, and 65 patients (90%) have so far undergone surgical correction, and of those, 35 (54%) have completed their treatment, the longest follow-up time being 18 years. The mean number of surgical procedures was 2.4, and 18 patients (28%) had postoperative complications, which included partial necrosis of the maxilla, osteomyelitis of the mandible, facial nerve and inferior alveolar nerve neuropraxia, nasal bone graft exposure, and cellulitis. DISCUSSION: Because of the phenotypic characteristics shared by both Binder syndrome and CDP, it is most likely that Binder syndrome is not a syndrome, nor is it an entity, but most likely to be an "association." We would advocate that these patients should be managed in a multidisciplinary setting.
Keywords: Binder syndrome
chondrodysplasia punctata
costochondral nasal grafts
Rights: © 2012 Mutaz B. Habal, MD
DOI: 10.1097/SCS.0b013e31824e2683
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