Two Cases of Axenfeld-Rieger Syndrome, Report of the Complex Pathology and Treatment

Céline Bender, Maarten Koudstaal, José Elswijk, B Andersen, Eppo Wolvius

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The purpose of this case report is to report the orthodontic surgical treatment and subsequent dental rehabilitation in two patients with Axenfeld-Rieger syndrome. Axenfeld-Rieger syndrome is a rare autosomal dominant condition characterized by ocular, dental, craniofacial, and periumbilical abnormalities. The treatment of two patients with various anomalies in Axenfeld-Rieger syndrome is described and discussed. Early recognition of the syndrome and referral during childhood to a specialized oral and maxillofacial surgery, special dental care, and orthodontic unit provide the optimal starting point for this complex treatment.
Original languageUndefined/Unknown
Pages (from-to)354-360
Number of pages7
JournalCleft Palate-Craniofacial Journal
Issue number3
Publication statusPublished - 2014

Research programs

  • EMC OR-01-59-01

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