Lacey D J, Terplan K
J Child Neurol. 1987 Jul;2(3):201-4. doi: 10.1177/088307388700200306.
A child born to a phenylketonuric (PKU) woman not on dietary treatment was microcephalic and had congenital heart and other physical anomalies consistent with the maternal PKU syndrome. After a repeat cardiac catherization at 3 months of age, he suffered an embolic left cerebral infarct and seizures. He was found by his mother dead in bed at 4 months of age; general autopsy revealed Klebsiella sepsis and pneumonia. Neuropathologic studies of the right cerebral hemisphere showed neuronal loss of the third cortical layer; Golgi studies revealed persistently immature cortical pyramidal cell somata and dendritic spines. This is the first report of specific neuronal abnormalities in a child with the maternal PKU syndrome and may, in part, account for the clinical features of microcephaly, mental retardation, and seizures seen in affected children.
一名未接受饮食治疗的苯丙酮尿症(PKU)女性所生的孩子患有小头畸形,并有与母体苯丙酮尿症综合征相符的先天性心脏病和其他身体异常。在3个月大时重复进行心脏导管插入术后,他发生了栓塞性左脑梗死并出现癫痫发作。他在4个月大时被母亲发现死在床上;全身尸检显示为克雷伯菌败血症和肺炎。右大脑半球的神经病理学研究显示第三皮质层神经元缺失;高尔基染色研究显示皮质锥体细胞的胞体和树突棘持续未成熟。这是关于患有母体苯丙酮尿症综合征儿童特定神经元异常的首次报告,可能部分解释了受影响儿童出现的小头畸形、智力迟钝和癫痫发作等临床特征。