Shaw D W, Weinberger E, Maravilla K R
Department of Radiology, University of Washington School of Medicine, Seattle 98195.
J Comput Assist Tomogr. 1990 May-Jun;14(3):458-60. doi: 10.1097/00004728-199005000-00026.
Phenylketonuria (PKU) is an autosomal recessive disease in which defects in phenylalanine metabolism result in hyperphenylalaninemia. Untreated patients generally have poor motor function and are profoundly retarded. We report a patient with PKU whose cranial magnetic resonance abnormalities correlate with known histopathologic changes. The ability to image the pathologic changes in PKU may have important implications regarding treatment and prognosis of these patients.
苯丙酮尿症(PKU)是一种常染色体隐性疾病,其中苯丙氨酸代谢缺陷导致高苯丙氨酸血症。未经治疗的患者通常运动功能较差且严重智力发育迟缓。我们报告了一名患有苯丙酮尿症的患者,其头颅磁共振成像异常与已知的组织病理学变化相关。对苯丙酮尿症病理变化进行成像的能力可能对这些患者的治疗和预后具有重要意义。