Kolar J C, Munro I R, Farkas L G
Humana Advanced Surgical Institutes, Medical City, Dallas, Texas 75230.
Am J Phys Anthropol. 1987 Dec;74(4):441-51. doi: 10.1002/ajpa.1330740403.
Advances in surgical techniques for correction of craniofacial anomalies have necessitated the development of objective pre- and postoperative quantitative assessments. Standard anthropometric techniques, supplemented by additional methods oriented to specific clinical problems, have proved useful in defining surface dysmorphology in craniofacial patients. A series of 77 surface measurements of the head and face and 41 proportions were determined in 20 preoperative patients with Treacher Collins syndrome, a rare congenital defect of the first and second branchial arches. To permit comparison with age- and sex-specific data for healthy North American children, the patient data were converted to standard (Z) scores. To test the hypothesis Z = 0, Student's t-test was performed on all variables. The anthropometric findings verified many of the clinical findings in this syndrome. In addition, a number of previously unreported defects were found. The cranium was low and short with a low, narrow forehead and a narrow cranial base. The face was narrow and shallow, the mandible long and narrow, and the lower face receding. The eye fissures were short with an antimongoloid inclination, but the orbits were hyperteloric. The nasal root was high and wide, the nasofrontal angle open, and the bridge inclination low. The labial fissure was narrow, and the ears were microtic. Except in the nasal root the defects were hypoplastic. Most of these defects were either horizontal or anteroposterior. Recognition of the defective areas and their contribution to disproportions of the head and face is important in the development of surgical strategies.
颅面畸形矫正手术技术的进步使得客观的术前和术后定量评估方法的开发成为必要。标准人体测量技术,辅以针对特定临床问题的其他方法,已被证明在定义颅面患者的表面畸形方面很有用。对20例患有特雷彻·柯林斯综合征(一种罕见的第一和第二鳃弓先天性缺陷)的术前患者进行了一系列77项头面部表面测量和41项比例测量。为了便于与北美健康儿童的年龄和性别特异性数据进行比较,将患者数据转换为标准(Z)分数。为了检验Z = 0的假设,对所有变量进行了学生t检验。人体测量结果证实了该综合征的许多临床发现。此外,还发现了一些以前未报告的缺陷。颅骨低而短,前额低而窄,颅底窄。面部窄而浅,下颌骨长而窄,下脸后缩。眼裂短,有反蒙古样倾斜,但眶距增宽。鼻根高而宽,鼻额角开放,鼻梁倾斜度低。唇裂窄,耳朵小。除鼻根外,这些缺陷均发育不全。这些缺陷大多是水平或前后方向的。识别缺陷区域及其对头部和面部比例失调的影响对于制定手术策略很重要。