Ludolph A C, Vetter U, Ullrich K
Department of Neurology, Humboldt University, Berlin, Germany.
Eur J Pediatr. 1996 Jul;155 Suppl 1:S64-8. doi: 10.1007/pl00014254.
We performed studies of multimodal evoked potentials and peripheral sensory and motor nerve conductions in 33 early and 6 late treated patients with phenylketonuria. The studies revealed the following picture: 1. In 27% of early treated patients latencies of visual evoked potentials were increased. The cause for these changes in unknown. 2. Nerve conduction studies showed the presence of a minor sensory neuropathy which in rare cases may also affect peripheral motor nerves. This neuropathy did not have features of a central-peripheral distal axonopathy which argues against a toxic/nutritional causation. 3. Deficits in the central sensory, motor, and auditory pathways were present, but rare in early treated patients. If the results of electrophysiological studies reported by different groups are compared, the emerging picture is very similar and the majority of the-minor-differences is likely to be explained by technical aspects.
我们对33例早期治疗和6例晚期治疗的苯丙酮尿症患者进行了多模态诱发电位以及外周感觉和运动神经传导研究。研究结果如下:1. 27%的早期治疗患者视觉诱发电位潜伏期延长。这些变化的原因不明。2. 神经传导研究显示存在轻度感觉神经病变,极少数情况下也可能影响外周运动神经。这种神经病变不具有中枢 - 外周远端轴索性神经病的特征,这排除了毒性/营养性病因。3. 中枢感觉、运动和听觉通路存在功能缺陷,但在早期治疗患者中较为少见。如果比较不同组报告的电生理研究结果,会发现呈现出的情况非常相似,大多数细微差异可能由技术因素解释。