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《雷特综合征的口腔表现:系统评价》。

Oral Manifestations of Rett Syndrome-A Systematic Review.

机构信息

Department of Community Dentistry, Jinnah Medical and Dental College, Sohail University, Karachi 74800, Pakistan.

Athena Center for Advanced Research in Healthcare, 62032 Camerino, Italy.

出版信息

Int J Environ Res Public Health. 2021 Jan 28;18(3):1162. doi: 10.3390/ijerph18031162.

DOI:10.3390/ijerph18031162
PMID:33525609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7908587/
Abstract

Rett Syndrome is an x linked developmental disorder which becomes apparent in females after 6 to 18 months of age. It leads to severe impairments including loss of speech, loss of hand movements/manual dexterity, characteristic hand movements such as hang wringing and intellectual disability/learning problems. This systematic review was carried out to identify the dental manifestation of Rett syndrome and to shed light on treatment options available for oral health problems associated with Rett syndrome. A systematic literature search was conducted on the PubMed, Scopus, Biomed, Web of Science, Embase, Google Scholars, Cochrane and CINAHL using the following entries: Rett syndrome ( = 3790), Oral health and Rett syndrome ( = 17), dental health of Rett syndrome patients ( = 13), and the MeSH terms listed below: Rett syndrome and Oral Health ( = 17), Rett syndrome and dentistry ( = 29). The final review included 22 search articles. The most common oral findings was bruxism. Masseteric hypertrophy was also reported. Anterior open bite and non-physiological tooth wear was observed. Other oral manifestations of Rett syndrome included mouth breathing, tongue thrusting, digit/thumb sucking, high arch palate. Increased awareness and dental education amongst dentists and assistants regarding the dental manifestations of Rett syndrome and similar neurodevelopmental disorders is required to improve the level of care and empathy they can provide to these differently able patients. Research on dental aspects of Rett is scarce and this remains a neglected topic.

摘要

雷特综合征是一种 X 连锁的发育障碍,在女性中于 6 至 18 个月龄后显现。它导致严重的损伤,包括丧失言语、丧失手部运动/手灵巧度、特征性手部动作如绞手以及智力残疾/学习问题。本系统综述旨在确定雷特综合征的口腔表现,并阐明与雷特综合征相关的口腔健康问题的治疗选择。在 PubMed、Scopus、Biomed、Web of Science、Embase、Google Scholar、Cochrane 和 CINAHL 上使用以下条目进行了系统文献检索:Rett 综合征(=3790)、口腔健康和雷特综合征(=17)、雷特综合征患者的口腔健康(=13)和以下 MeSH 术语:Rett 综合征和口腔健康(=17)、Rett 综合征和牙科(=29)。最终综述纳入了 22 篇检索文章。最常见的口腔发现是磨牙症。也有报道称咀嚼肌肥大。观察到前牙开颌和非生理性牙齿磨损。雷特综合征的其他口腔表现包括张口呼吸、舌前突、手指/拇指吸吮、高拱形腭。提高牙医和助手对雷特综合征和类似神经发育障碍的口腔表现的认识和口腔教育,以提高他们对这些有特殊需要的患者的护理和同理心水平。关于雷特综合征牙科方面的研究很少,这仍然是一个被忽视的话题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d34/7908587/973a5605219c/ijerph-18-01162-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d34/7908587/9266d1d31dde/ijerph-18-01162-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d34/7908587/973a5605219c/ijerph-18-01162-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d34/7908587/9266d1d31dde/ijerph-18-01162-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d34/7908587/973a5605219c/ijerph-18-01162-g002.jpg

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