Najjar Dany M, Christiansen Stephen P, Bothun Erick D, Summers C Gail
Department of Ophthalmology, University of Minnesota, Minneapolis, Minnesota 55455, USA.
J AAPOS. 2006 Jun;10(3):193-7. doi: 10.1016/j.jaapos.2006.01.006.
Peters anomaly is a rare form of anterior segment dysgenesis in which abnormal cleavage of the anterior chamber occurs at the end of the third week of gestation. We examined the prevalence of strabismus and amblyopia and analyzed predictive factors for their development, as well as the visual outcome and associated anomalies in patients with bilateral Peters anomaly.
Using a retrospective review, we identified 25 consecutive patients with bilateral Peters anomaly who were observed between August 1995 and February 2005. Ocular structural and systemic anomalies, amblyopia therapy, visual acuity, and binocular alignment at last visit were recorded. Fisher's exact test was used to identify any association between defined predictive factors and the development of strabismus.
Mean follow-up time was 5.1 year (range, 0.5-21 years). Median age at presentation was 2.5 months (range, 1 day to 13 years). Penetrating keratoplasties were performed on 34 eyes in 20 patients. Final best-corrected visual acuity ranged from 20/25 to no light perception. Thirteen of 18 patients with recorded motility (72%) developed strabismus: esotropia (n = 7), exotropia (n = 5), and variable (n = 1); one also had dissociated vertical deviation. Patients with equal vision were either orthophoric (n = 4) or had intermittent esotropia (n = 1), whereas strabismus occurred in 100% of patients whose vision was asymmetric by more than 1.5 octaves. Asymmetric vision was the only statistically significant predictive factor for the development of strabismus (P = 0.002). Amblyopia treatment resulted in improved vision in 3 of 5 patients.
Strabismus occurs frequently in bilateral Peters anomaly. Asymmetric vision, (because of ocular structural anomalies) postoperative complications, and amblyopia may predispose to strabismus. Despite ocular structural limitations, amblyopia therapy is recommended in the aggressive rehabilitation of these eyes.
彼得斯异常是一种罕见的眼前节发育异常形式,在妊娠第三周结束时前房出现异常分隔。我们研究了斜视和弱视的患病率,分析了其发生的预测因素,以及双侧彼得斯异常患者的视力结果和相关异常情况。
通过回顾性研究,我们确定了1995年8月至2005年2月期间连续观察的25例双侧彼得斯异常患者。记录了眼部结构和全身异常、弱视治疗、视力以及最后一次就诊时的双眼视轴矫正情况。采用费舍尔精确检验来确定特定预测因素与斜视发生之间的任何关联。
平均随访时间为5.1年(范围0.5 - 21年)。就诊时的中位年龄为2.5个月(范围1天至13岁)。20例患者的34只眼进行了穿透性角膜移植术。最终最佳矫正视力范围从20/25至无光感。记录有眼球运动情况的18例患者中有13例(72%)发生了斜视:内斜视(n = 7)、外斜视(n = 5)和混合型(n = 1);1例还伴有分离性垂直偏斜。视力相等的患者要么为正位(n = 4),要么有间歇性内斜视(n = 1),而视力不对称超过1.5个倍频程的患者中100%发生了斜视。视力不对称是斜视发生的唯一具有统计学意义的预测因素(P = 0.002)。5例患者中有3例弱视治疗后视力得到改善。
斜视在双侧彼得斯异常中频繁发生。视力不对称(由于眼部结构异常)、术后并发症和弱视可能易导致斜视。尽管存在眼部结构限制,但对于这些眼睛的积极康复治疗仍建议进行弱视治疗。