Heliövaara A, Hurmerinta K
Department of Plastic Surgery, Cleft Center, Helsinki University Central Hospital, HUS, Finland.
Orthod Craniofac Res. 2006 Nov;9(4):186-92. doi: 10.1111/j.1601-6343.2006.00373.x.
To evaluate cephalometrically the craniofacial, pharyngeal and cervical morphology in children with CATCH 22, and to compare and quantify the findings with age- and sex-matched controls.
A retrospective case-control study.
Forty-one children (20 girls) with CATCH 22 were compared with age- and sex-matched controls from lateral cephalograms taken at the mean age of 8.5 years (range 5.8-12.9). The deletion of 22q11 was verified by fluorescence in situ hybridization techniques. Thirteen of the children with CATCH 22 had palatal clefts.
Linear and angular measurements were obtained from lateral cephalograms. A Student's t-test and a paired Student's t-test were used in the statistical analysis. Standard deviation scores (SDS) were calculated to quantify the variation.
Children with CATCH 22 had obtuse cranial base angles and long anterior cranial bases. Their faces were long with increased facial convexity. The maxillae were long but both jaws were retrognathic and the lower jaws posteriorly diverged. The pharynges were wide in the nasopharyngeal area and narrow in the hypopharyngeal area. The development of the hyoid bones was delayed, and hyoid bone and atlas lengths were reduced. The morphology of the children with CATCH 22 with and without a palatal cleft was similar. Despite several statistically significant differences between the children with CATCH 22 and the controls, the SDS did not exceed +/-2 for any of the measurements.
Children with CATCH 22 have several minor distinctive morphological features in the craniofacial, pharyngeal, and cervical areas.
通过头影测量法评估患有22q11.2微缺失综合征(CATCH 22)的儿童的颅面、咽部和颈部形态,并将结果与年龄和性别匹配的对照组进行比较和量化。
一项回顾性病例对照研究。
将41名患有CATCH 22的儿童(20名女孩)与年龄和性别匹配的对照组进行比较,这些对照来自平均年龄8.5岁(范围5.8 - 12.9岁)时拍摄的头颅侧位片。通过荧光原位杂交技术验证22q11的缺失。41名患有CATCH 22的儿童中有13名患有腭裂。
从头颅侧位片中获取线性和角度测量值。统计分析采用学生t检验和配对学生t检验。计算标准差分数(SDS)以量化差异。
患有CATCH 22的儿童颅底角钝,前颅底长。他们的脸长,面部凸度增加。上颌骨长,但上下颌均后缩,下颌后向散开。咽部在鼻咽区域宽,在下咽区域窄。舌骨发育延迟,舌骨和第一颈椎长度缩短。患有和未患有腭裂的CATCH 22儿童的形态相似。尽管患有CATCH 22的儿童与对照组之间存在一些统计学上的显著差异,但任何测量的SDS均未超过±2。
患有CATCH 22的儿童在颅面、咽部和颈部区域有一些轻微的独特形态特征。