Barashnev Y I, Korneichuk V V, Klembovsky A I, Klyushina L A
J Inherit Metab Dis. 1982;5(4):204-10. doi: 10.1007/BF02179142.
Comprehensive studies on structure and function of the liver (biochemical profiles, light and electron microscopy, determination of phenylalanine hydroxylase activity) were performed in children with phenylketonuria (PKU). It was established that the liver is always involved in the pathological process. Comparison of results obtained with peculiarities of neuropsychiatric disorders revealed a dependence of the initial manifestations and the severity of PKU on the extent of enzyme deficiency. Amino acid disorders and abnormal lipid metabolism both contribute to the genesis of cerebral lesions.
对苯丙酮尿症(PKU)患儿的肝脏结构和功能进行了全面研究(生化指标、光镜和电镜检查、苯丙氨酸羟化酶活性测定)。结果表明肝脏总是参与到病理过程中。将所得结果与神经精神障碍的特点进行比较后发现,PKU的初始表现和严重程度取决于酶缺乏的程度。氨基酸紊乱和脂质代谢异常均促成脑损伤的发生。