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唐氏综合征导致颅面区域异常:系统文献回顾。

Down syndrome as a cause of abnormalities in the craniofacial region: A systematic literature review.

机构信息

Department of Dentofacial Orthopaedics and Orthodontics, Division of Facial Abnormalities, Wroclaw Medical University, Poland.

Department of Ophthalmology, Kalmedica, Kalisz, Poland.

出版信息

Adv Clin Exp Med. 2019 Nov;28(11):1587-1592. doi: 10.17219/acem/112785.

DOI:10.17219/acem/112785
PMID:31778604
Abstract

Down syndrome (DS) is the most often diagnosed chromosomal disorder in newborns. The incidence is 1:792 live births. The article describes the irregularities and characteristics found in trisomy 21, which greatly affect the functioning of the stomatognathic system. The most significant disorders include the following: false macroglossia, muscular hypotonia and gothic palate. These abnormalities affect articulation, breathing, food intake, and swallowing. We analyzed the morphological characteristics of the craniofacial region in children with DS based on the current literature review. The following databases were used for the analysis: MEDLINE (via PubMed), Scopus, Infona, and Dentistry & Oral Sciences Source. In the course of the study, 199 pieces of literature were analyzed; the analysis also included 18 articles on children and adults with DS. It also took into account the structure of the palate, dental and skeletal defects, size of the tongue, muscular hypotonia, and temporomandibular joint dysfunction. Down syndrome is still a current subject of research. Although macroglossia, hypotonia, malocclusion, and temporomandibular joint abnormalities are not features exclusive to DS, numerous dysfunctions and parafunctions as well as retarded psychomotor development greatly complicate the treatment. Therefore, interdisciplinary treatment of patients with trisomy 21 and early treatment in the first months of life with the use of the Castillo-Morales plate are very important, as they ensure better adaptation to the subsequently used apparatus and reduce the risk of disorders of the stomatognathic system.

摘要

唐氏综合征(DS)是新生儿中最常见的染色体疾病。发病率为 1:792 活产。本文描述了 21 三体综合征中发现的不规则和特征,这些不规则和特征极大地影响了口腔颌系统的功能。最显著的异常包括以下内容:假性巨舌、肌肉张力减退和哥特式腭。这些异常影响发音、呼吸、进食和吞咽。我们根据当前的文献综述分析了 DS 儿童的头面部形态特征。分析使用了以下数据库:MEDLINE(通过 PubMed)、Scopus、Infona 和 Dentistry & Oral Sciences Source。在研究过程中,分析了 199 篇文献;分析还包括 18 篇关于儿童和成人 DS 的文章。还考虑了腭的结构、牙齿和骨骼缺陷、舌的大小、肌肉张力减退和颞下颌关节功能障碍。唐氏综合征仍然是一个当前的研究课题。尽管巨舌、张力减退、错颌和颞下颌关节异常不是 DS 所特有的特征,但许多功能和功能障碍以及运动发育迟缓极大地增加了治疗的复杂性。因此,对 21 三体综合征患者进行跨学科治疗以及在生命的头几个月使用 Castillo-Morales 板进行早期治疗非常重要,因为它们可以确保更好地适应随后使用的器具,并降低口腔颌系统障碍的风险。

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Down syndrome as a cause of abnormalities in the craniofacial region: A systematic literature review.唐氏综合征导致颅面区域异常:系统文献回顾。
Adv Clin Exp Med. 2019 Nov;28(11):1587-1592. doi: 10.17219/acem/112785.
2
Long term effects of the palatal plate therapy for the orofacial regulation in children with Down syndrome.腭板治疗对唐氏综合征患儿口面部功能调节的长期影响。
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