Giovannini M, Valsasina R, Villani R, Ducati A, Riva E, Landi A, Longhi R
Clinica Pediatrica V, Istituto di Scienze Biomediche, Milano.
J Inherit Metab Dis. 1988;11(4):416-21. doi: 10.1007/BF01800430.
The pathogenesis of brain dysfunction in phenylketonuria (PKU) is still under investigation. Hyperphenylalaninaemia results in increased turnover of myelin. In order to demonstrate the derangement of myelinization in PKU we studied the visual evoked potentials (VEP) in 14 PKU patients and in 20 normal subjects. VEP findings were correlated with the metabolic control of the disease and with the electroencephalographic findings. VEP were more sensitive than the EEG in detecting a neurological dysfunction. VEP are influenced by dietary control and are normal only in children with good metabolic control.
苯丙酮尿症(PKU)脑功能障碍的发病机制仍在研究中。高苯丙氨酸血症导致髓鞘更新增加。为了证明PKU患者髓鞘形成的紊乱,我们研究了14例PKU患者和20名正常受试者的视觉诱发电位(VEP)。VEP结果与疾病的代谢控制及脑电图结果相关。在检测神经功能障碍方面,VEP比脑电图更敏感。VEP受饮食控制影响,仅在代谢控制良好的儿童中正常。