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17例黏多糖贮积症VI型患者的口腔表现

Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI.

作者信息

Kantaputra Piranit Nik, Kayserili Hülya, Güven Yeliz, Kantaputra Warissara, Balci Mehmet C, Tanpaiboon Pranoot, Uttarilli Anusha, Dalal Ashwin

机构信息

Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry; Craniofacial Genetics Laboratory, Faculty of Dentistry, Chiang Mai University, Chiang Mai, Thailand,

出版信息

J Inherit Metab Dis. 2014 Mar;37(2):263-8. doi: 10.1007/s10545-013-9645-8. Epub 2013 Aug 22.

Abstract

OBJECTIVE

To assess oral manifestations of 17 patients with mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome.

METHODS

We performed comprehensive oral examinations in 17 patients with MPS VI. Panoramic radiographs was performed only in 14 patients. All patients were of Thai, Turkish, and Indian origins. Ten of 17 patients had enzyme replacement therapy (ERT) (Naglazyme). Most Turkish patients (10/11) were on ERT. The Thai and Indian patients have never had ERT.

RESULTS

Oral and radiographic examinations showed that hypoplastic mandibular condyles (93.3 %), malposition of unerupted teeth (92.9 %), large dental follicles (92.3 %), anterior open bite (86.7 %), maxillary constriction (56.3 %), and taurodontism (53.8 %) were common among patients with MPS VI. Newly recognized oral findings found in our study included taurodontism, long tooth roots, abnormal frenum, missing teeth, supernumerary teeth, and microdontia. Two patients who started ERT prior to 3 years old did not develope anterior open bite and one of them had mildly affected mandibular condyles.

CONCLUSION

Our study provides the most comprehensive study of oral manifestations in patients with MPS VI. Receiving ERT at very young ages may lessen craniofacial malformations including hypoplasic mandibular condyles and anterior open bite. Oral manifestations can be used as diagnostic features for MPS VI prior to assessing leukocyte ARSB activity or urinary excretion of dermatan sulfate.

摘要

目的

评估17例黏多糖贮积症VI型(MPS VI)或马罗泰克斯-拉米综合征患者的口腔表现。

方法

我们对17例MPS VI患者进行了全面的口腔检查。仅14例患者拍摄了全景X线片。所有患者来自泰国、土耳其和印度。17例患者中有10例接受了酶替代疗法(ERT)(Naglazyme)。大多数土耳其患者(10/11)接受了ERT。泰国和印度患者从未接受过ERT。

结果

口腔和影像学检查显示,发育不全的下颌髁突(93.3%)、未萌出牙错位(92.9%)、大的牙囊(92.3%)、前牙开颌(86.7%)、上颌狭窄(56.3%)和牛牙症(53.8%)在MPS VI患者中很常见。我们的研究中新发现的口腔表现包括牛牙症、长牙根、异常系带、牙齿缺失、多生牙和过小牙。2例在3岁前开始接受ERT的患者未出现前牙开颌,其中1例下颌髁突轻度受累。

结论

我们的研究提供了对MPS VI患者口腔表现最全面的研究。在非常小的年龄接受ERT可能会减轻颅面畸形,包括下颌髁突发育不全和前牙开颌。在评估白细胞ARSB活性或硫酸皮肤素尿排泄之前,口腔表现可作为MPS VI的诊断特征。

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