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Oral manifestation and root canal therapy of the patient with mucopolysaccharidosis

机译:黏多糖贮积症患者的口腔表现和根管治疗

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摘要

Mucopolysaccharidosis (MPS) is an inherited metabolic disorder caused by a deficiency in enzymes that participate in the degradation of glycosaminoglycans (GAGs) such as heparin sulfate and dermatan sulfate. Left untreated, patients show progressive mental and physical deterioration due to deposition of GAGs in organs. Death often occurs due to cardiac or respiratory failure before patients reach their early twenties. MPS has several oral and dental manifestations. An enlarged head, short neck, and open mouth associated with a large tongue are major characteristics of MPS patients. Dental complications can be severe, including unerupted dentition, dentigerous cyst-like follicles, malocclusions, condylar defects, and gingival hyperplasia. A 21-year-old female patient with MPS was described in this article, with special emphasis on oral manifestations and dental treatment.
机译:粘多糖贮积病(MPS)是一种遗传性代谢紊乱,是由参与糖胺聚糖(GAG)降解的酶(例如硫酸肝素和硫酸皮肤素)缺乏引起的。如果不及时治疗,由于GAGs沉积在器官中,患者会出现进行性的精神和身体恶化。死亡通常是由于心脏衰竭或呼吸衰竭而导致的,直到患者二十多岁。 MPS有几种口腔和牙齿表现。 MPS患者的主要特征是头部增大,颈部短,嘴巴张大。牙齿并发症可能很严重,包括牙列未裂,囊肿样囊性卵泡,错牙合畸形,con突缺损和牙龈增生。本文介绍了一名21岁的MPS女性患者,其中特别强调了口腔表现和牙科治疗。

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