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Title: Distraction in a case of otopalatodigital syndrome type II. Author: Batra P, Ryan FS, Witherow H, Calvert ML. Journal: Int J Paediatr Dent; 2006 Jul; 16(4):286-91. PubMed ID: 16759327. Abstract: INTRODUCTION: Otopalatodigital syndrome type II is a rare X-linked recessive disorder with generalized skeletal dysplasia and hearing anomalies. Its features include conductive hearing loss, unusual facies, cleft palate, micrognathia, and overlapping flexed fingers and toes. It is a more lethal variant of otopalatodigital syndrome type I. There are many consistently reported craniofacial and dental findings; however, no case has been published in dental literature. CASE REPORT: We report a case of otopalatodigital syndrome type II with micrognathia, cleft of the soft palate, and partial anodontia, and discuss the combined orthodontic and surgical management. CONCLUSION: We also discuss the differential diagnosis and consider more recent theories on possible aetiology as well as clinical management strategies for such cases.[Abstract] [Full Text] [Related] [New Search]