Kelly John P, Ishak Gisele E, Phillips James O, Nguyen Ho, Weiss Avery H
Roger H. Johnson Vision Lab, Division of Ophthalmology, Seattle Children's Hospital, Seattle, Washington; Department of Ophthalmology, University of Washington Medical Center, Seattle.
Division of Radiology, Seattle Children's Hospital, Seattle, Washington; Department of Radiology, University of Washington Medical Center, Seattle.
J AAPOS. 2016 Feb;20(1):37-43. doi: 10.1016/j.jaapos.2015.10.016.
To assess visual and ocular motor function in children with polymicrogyria (PMG).
The medical records of 15 children (0.4-4 years of age) with PMG documented by magnetic resonance imaging (MRI) and with age-corrected visual acuity measured by Teller acuity cards were reviewed retrospectively. Cortical function was assessed by pattern visually evoked potentials (VEP). Ocular motor function was assessed by video-oculography or clinical assessment. Results were compared to age-matched controls.
Extent of PMG involvement varied from bilateral fronto-parietal to bilateral-diffuse. Nine children had involvement of the occipital lobe. Visual acuity at presentation was normal in 5 children (≥20/40 Snellen equivalent for age) and subnormal in 10 (average 20/200 equivalent). Visual acuity was similar in children with or without involvement of the occipital lobe (P = 0.4). Follow-up visual acuity was available for 9 children; 3 improved and 6 failed to improve (5 of whom had seizures). PMG involving the occipital lobe significantly reduced VEP amplitude and signal-to-noise ratios. Three infants without visually-guided behaviors had VEP responses. All 3 children with cytomegalovirus-related PMG without retinal disease had preserved visual function despite generalized MRI abnormalities.
All children with PMG had recordable visual function either by visual acuity or VEP testing, however the majority did not show longitudinal improvement in acuity. Seizures may impose limits on visual acuity development. Children with cytomegalovirus-related PMG, microcephaly, and developmental delay can have normal visual acuity. Children with a recordable VEP but without visually guided behaviors may have a defect in sensorimotor transformation.
评估多小脑回畸形(PMG)患儿的视觉和眼球运动功能。
回顾性分析15例经磁共振成像(MRI)确诊为PMG且通过泰勒视力卡测量了年龄校正视力的儿童(0.4 - 4岁)的病历。通过图形视觉诱发电位(VEP)评估皮质功能。通过视频眼动图或临床评估评估眼球运动功能。将结果与年龄匹配的对照组进行比较。
PMG的累及范围从双侧额顶叶到双侧弥漫性不等。9例患儿累及枕叶。就诊时5例患儿视力正常(年龄相当于Snellen视力表≥20/40),10例患儿视力低于正常(平均相当于20/200)。枕叶受累与未受累患儿的视力相似(P = 0.4)。9例患儿有随访视力;3例改善,6例未改善(其中5例有癫痫发作)。累及枕叶的PMG显著降低VEP波幅和信噪比。3例无视觉引导行为的婴儿有VEP反应。所有3例与巨细胞病毒相关的PMG且无视网膜疾病的患儿尽管MRI有广泛异常,但视觉功能均保留。
所有PMG患儿通过视力或VEP测试均有可记录的视觉功能,然而大多数患儿的视力在纵向随访中未显示改善。癫痫发作可能会限制视力发育。与巨细胞病毒相关的PMG、小头畸形和发育迟缓的患儿可能有正常视力。有可记录的VEP但无视觉引导行为的患儿可能存在感觉运动转换缺陷。