Macintosh Claire, Wall Steve, Leach Carolyn
Oxford Craniofacial Unit, Oxford Radcliffe Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
J Craniofac Surg. 2007 May;18(3):465-9. doi: 10.1097/scs.0b01e3180515d94.
Unicoronal synostosis is a premature fusion of one of the coronal sutures and is thought to carry an increased prevalence for strabismus. Studies suggest the nature of the strabismus to be a hypertropia occurring ipsilateral to the fused coronal suture. The aim of this study is to investigate the laterality of strabismus in unicoronal synostosis and report on ocular motility and refractive findings in a large, unbiased sample group. A retrospective case study analysis was carried out on 59 patients with a confirmed diagnosis of unicoronal synostosis referred to the Oxford Craniofacial Unit over a 14 year period. Manifest strabismus in the primary position was found in 34 (57.6%) cases. In 19 (55.9%) cases, this occurred contralateral to the fused suture, and in 9 (26.5%) cases, strabismus was on the ipsilateral side. Six had alternating strabismus. These results are contrary with apparent findings in the literature but are not statistically significant (P = 0.0872) for strabismus occurring more frequently on the nonsynostotic side. Esotropia with a vertical component was most common, found in 61% of all cases with strabismus. Apparent inferior oblique overaction was found in 30 of the 59 (50.8%) cases, with this occurring bilaterally in 14 cases. Significant refractive error was found in 46% of all cases, most of which showed anisometropia and astigmatism that occurred more frequently on the contralateral, nonsynostotic side (P = 0.0106). All cases of unicoronal synostosis with a mutation of the FGFR2 or FGFR3 gene had manifest strabismus. Manifest strabismus was found in 57.6% of cases reviewed, but this was found to be no more likely to occur on the side contralateral or ipsilateral to the fused suture (P = 0.0872). Anisometropia and astigmatism were found more frequently in the eye contralateral to the fused suture.
单冠状缝早闭是指冠状缝之一过早融合,被认为斜视患病率增加。研究表明,斜视的性质是与融合冠状缝同侧发生的上斜视。本研究的目的是调查单冠状缝早闭中斜视的偏向性,并报告一个大型、无偏倚样本组的眼球运动和屈光检查结果。对14年间转诊至牛津颅面科的59例确诊为单冠状缝早闭的患者进行了回顾性病例研究分析。在34例(57.6%)患者中发现了原在位的显性斜视。其中19例(55.9%)发生在与融合缝对侧,9例(26.5%)斜视在同侧。6例为交替性斜视。这些结果与文献中的明显发现相反,但对于斜视在非融合侧更频繁发生这一情况,差异无统计学意义(P = 0.0872)。伴有垂直成分的内斜视最为常见,在所有斜视病例中占61%。在59例(50.8%)患者中有30例发现明显的下斜肌亢进,其中14例为双侧。46%的患者存在明显的屈光不正,其中大多数表现为屈光参差和散光,且在对侧非融合侧更常见(P = 0.0106)。所有FGFR2或FGFR3基因突变的单冠状缝早闭病例均有显性斜视。在回顾的病例中,57.6%有显性斜视,但发现在融合缝对侧或同侧发生的可能性并无差异(P = 0.0872)。屈光参差和散光在与融合缝对侧的眼睛中更常见。