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18例与SATB2相关综合征患者的口腔影像学表现。

Dental radiographic findings in 18 individuals with SATB2-associated syndrome.

作者信息

Scott John, Adams Chad, Simmons Kirt, Feather Andrea, Jones John, Hartzell Larry, Wesley Lucia, Johnson Adam, Fish Jennifer, Bosanko Katherine, Beetstra Stephen, Zarate Yuri A

机构信息

Center for Dental Education, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

Department of Surgery, Plastic and Reconstructive Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

出版信息

Clin Oral Investig. 2018 Nov;22(8):2947-2951. doi: 10.1007/s00784-018-2702-9. Epub 2018 Oct 12.

DOI:10.1007/s00784-018-2702-9
PMID:30315422
Abstract

OBJECTIVE

To characterize the radiographic dental phenotype of individuals with SATB2-associated syndrome (SAS).

MATERIALS AND METHODS

Participants were evaluated by a multidisciplinary team during a concurrent clinic conducted during the 1st international SAS family meeting held in 2017 at a single institution. Whenever possible, panoramic and/or periapical radiographs were obtained in clinic or previously obtained and provided by the caregiver.

RESULTS

Of the 37 individuals evaluated, 18 (12 males, median age 8.5 years) underwent radiographic examination. Dental radiographs revealed anomalies in all individuals starting at 2 years of age. The most consistent finding was delayed development of the mandibular second bicuspids (83%) with other common radiographic findings including delayed development of the roots of the permanent teeth (78%), severely rotated (56%) or malformed teeth (44%), and taurodontism (44%).

CONCLUSIONS

Dental anomalies are fully penetrant and can be documented radiographically in all individuals with SAS.

CLINICAL RELEVANCE

Dental radiographic findings of delayed second premolar development and delayed development of permanent root formation, especially concurrent with findings of taurodontism and malformed teeth, support a clinical suspicion for SAS and should help differentiate SAS from other neurodevelopmental syndromes.

摘要

目的

描述SATB2相关综合征(SAS)患者的口腔X线表现型。

材料与方法

在2017年于单一机构举行的第一届国际SAS家族会议同期诊所期间,由多学科团队对参与者进行评估。只要有可能,就在诊所获取全景和/或根尖片,或者由照料者提供之前获取的片子。

结果

在接受评估的37名个体中,18名(12名男性,中位年龄8.5岁)接受了口腔X线检查。口腔X线片显示所有个体在2岁时就出现了异常。最常见的表现是下颌第二双尖牙发育延迟(83%),其他常见的口腔X线表现包括恒牙牙根发育延迟(78%)、严重扭转(56%)或牙齿畸形(44%)以及牛牙症(44%)。

结论

牙齿异常具有完全外显率,并且在所有SAS患者中都可以通过X线片记录下来。

临床意义

第二前磨牙发育延迟和恒牙牙根形成延迟的口腔X线表现,特别是与牛牙症和牙齿畸形同时出现时,支持对SAS的临床怀疑,并且有助于将SAS与其他神经发育综合征区分开来。

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Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome.72例SATB2相关综合征患者的自然病史及基因型-表型相关性
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Alterations in Tooth Structure and Associated Systemic Conditions.牙齿结构改变及相关全身状况
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Genetic analysis of a child with ‑associated syndrome and literature study.一名患有[相关综合征名称]儿童的基因分析及文献研究。 (你原文中“‑associated syndrome”处相关综合征名称缺失,请补充完整准确信息以便更精准翻译)
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The dental phenotype of primary dentition in SATB2-associated syndrome: a report of three cases and literature review.SATB2 相关综合征患者乳牙列的牙体表型:三例报告及文献复习。
BMC Oral Health. 2022 Nov 22;22(1):522. doi: 10.1186/s12903-022-02594-4.
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A novel mutation of SATB2 inhibits odontogenesis of human dental pulp stem cells through Wnt/β-catenin signaling pathway.一种新型 SATB2 突变通过 Wnt/β-catenin 信号通路抑制人牙髓干细胞的成牙本质分化。
Stem Cell Res Ther. 2021 Dec 4;12(1):595. doi: 10.1186/s13287-021-02660-8.
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Special AT-rich sequence-binding protein 2 (Satb2) synergizes with Bmp9 and is essential for osteo/odontogenic differentiation of mouse incisor mesenchymal stem cells.富含特殊 AT 序列结合蛋白 2(Satb2)与 Bmp9 协同作用,对于小鼠切牙间充质干细胞的成骨/成牙分化是必不可少的。
Cell Prolif. 2021 Apr;54(4):e13016. doi: 10.1111/cpr.13016. Epub 2021 Mar 4.
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