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下颌面骨发育不全综合征患者颅面形态的头影测量评估

Cephalometric assessment of craniofacial morphology in patients with treacher Collins syndrome.

作者信息

Kapadia Hitesh, Shetye Pradip R, Grayson Barry H, McCarthy Joseph G

机构信息

Craniofacial Center, Seattle Children's Hospital, Seattle, WA, USA.

出版信息

J Craniofac Surg. 2013 Jul;24(4):1141-5. doi: 10.1097/SCS.0b013e3182860541.

Abstract

BACKGROUND AND PURPOSE

Treacher Collins syndrome is an autosomal dominant craniofacial disorder affecting derivatives of the first and second branchial arches. Given the conflicting reports in the literature regarding the extent of anterior-posterior and vertical (superior-inferior) dysplasia of the cranial base, maxilla, and mandible, this study was designed to provide a comprehensive lateral cephalometric assessment of the craniofacial morphology of unoperated patients with Treacher Collins syndrome.

METHODS

The records of 45 patients with Treacher Collins syndrome registered at the Institute of Reconstructive Plastic Surgery of the NYU Langone Medical Center from the period of 1975 to 2008 were reviewed. Inclusion criteria included (1) patients between with the ages of 5 and 17 years, (2) no history of prior surgical intervention to correct skeletal deformity, and (3) diagnostic quality lateral cephalograms. Twenty patients satisfied the inclusion criteria with 12 male and 8 female patients in the sample and a mean age at the time of the lateral cephalogram of 8.8 years (range 5.2 to 16.7 years). Thirty angular and linear variables were measured to assess anterior-posterior and vertical (superior-inferior) position of the cranial base, maxilla, and mandible. Each patient's measurements were compared to age-matched and sex-matched control samples derived from the Moyers growth studies. The mean and standard deviation for each variable was then determined.

RESULTS

Lateral cephalometric analysis showed decreased anterior, posterior, and total cranial base lengths and a reduced cranial base angle. The anteroposterior dimension or length of the maxilla is deficient and the maxilla is positioned posteriorly with respect to the cranial base. Both anterior and posterior facial heights (superior-inferior dimension) are decreased. Lower face height is increased, whereas total face is decreased. The maxillary and functional occlusal planes are tipped upwards posteriorly. The mandibular morphology is characteristically small in both body length and total mandibular length, and the maximum ramus width is also deficient. The mandibular plane angle and gonial angle are increased. The mandible is retropositioned.

CONCLUSIONS

A lateral cephalometric analysis is described that provides a skeletal basis for the hallmark clinical findings associated with Treacher Collins syndrome. This is of importance because an understanding of the underlying skeletal dysmorphology may shed light on the etiology and growth pattern, and impacts the overall treatment planning for skeletal correction.

摘要

背景与目的

特雷彻·柯林斯综合征是一种常染色体显性颅面疾病,影响第一和第二鳃弓的衍生物。鉴于文献中关于颅底、上颌骨和下颌骨前后及垂直(上下)发育异常程度的报道相互矛盾,本研究旨在对未经手术治疗的特雷彻·柯林斯综合征患者的颅面形态进行全面的侧位头影测量评估。

方法

回顾了1975年至2008年在纽约大学朗格尼医学中心重建整形外科学院登记的45例特雷彻·柯林斯综合征患者的记录。纳入标准包括:(1)年龄在5至17岁之间的患者;(2)无先前手术矫正骨骼畸形的病史;(3)具有诊断质量的侧位头影测量片。20例患者符合纳入标准,样本中有12例男性和8例女性患者,侧位头影测量时的平均年龄为8.8岁(范围5.2至16.7岁)。测量了30个角度和线性变量,以评估颅底、上颌骨和下颌骨的前后及垂直(上下)位置。将每位患者的测量结果与来自莫耶斯生长研究的年龄匹配和性别匹配的对照样本进行比较。然后确定每个变量的平均值和标准差。

结果

侧位头影测量分析显示,颅底的前后及总长度减小,颅底角减小。上颌骨的前后尺寸或长度不足,且相对于颅底向后移位。面部的前后高度(上下尺寸)均减小。下面高增加,而全面高减小。上颌和功能性咬合平面向后向上倾斜。下颌骨形态在体长和下颌骨总长度方面均较小,且最大升支宽度也不足。下颌平面角和下颌角增加。下颌骨后缩。

结论

描述了一种侧位头影测量分析方法,该方法为与特雷彻·柯林斯综合征相关的标志性临床发现提供了骨骼基础。这很重要,因为了解潜在的骨骼畸形可能有助于揭示病因和生长模式,并影响骨骼矫正的整体治疗计划。

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