Smith K S, Hallett K B, Hall R K, Wardrop R W, Firth N
Department of Plastic and Maxillofacial Surgery, Royal Children's Hospital, Melbourne, Australia.
Int J Oral Maxillofac Surg. 1995 Apr;24(2):176-80. doi: 10.1016/s0901-5027(06)80097-4.
Eight cases of mucopolysaccharidosis Type VI (Maroteaux-Lamy syndrome) are reviewed and two cases are presented in detail. Developmental dental anomalies including unerupted and impacted permanent teeth and associated hyperplastic tooth follicles are seen frequently in MPS patients. The surgical implications and management are discussed. All patients reviewed had significant cardiovalvular disease. It is essential for the primary medical provider to establish early basic dental care and evaluation for delayed eruption of primary and permanent dentition. This will probably minimize the possibility of infective endocarditis and allow for early treatment of impacted teeth.
回顾了8例VI型黏多糖贮积症(马罗-拉米综合征),并详细介绍了2例。发育性牙齿异常,包括恒牙未萌出和阻生以及相关的增生性牙滤泡,在黏多糖贮积症患者中很常见。讨论了手术意义和处理方法。所有接受回顾的患者都有严重的心瓣膜疾病。对于初级医疗提供者来说,为乳牙和恒牙萌出延迟建立早期基本牙科护理和评估至关重要。这可能会最大限度地降低感染性心内膜炎的可能性,并允许对阻生牙进行早期治疗。