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Title: Common dental features and craniofacial development of three siblings with Ter Haar syndrome. Author: Parker K, Pabla R, Hay N, Ayliffe P. Journal: Eur Arch Paediatr Dent; 2014 Feb; 15(1):59-64. PubMed ID: 24085649. Abstract: BACKGROUND: Ter Haar syndrome is a rare genetic syndrome with <30 cases reported worldwide. There is nothing within the published literature regarding the dental development and dental features of these patients. CASE REPORT: This case series examines three patients with Ter Haar syndrome and tracks their dental development and identifies common dental and skeletal features. FOLLOW-UP: All three patients received dental treatment and regular follow-up at Great Ormond Street Hospital Dental Department. CONCLUSION: These patients have many common dental and craniofacial features which poses the question as to whether these features are due to Ter Haar syndrome.[Abstract] [Full Text] [Related] [New Search]