Dobyns W B
Department of Neurology, Medical College of Wisconsin, Milwaukee.
Neurology. 1989 Jun;39(6):817-20. doi: 10.1212/wnl.39.6.817.
A 2-week-old infant who presented with myoclonic encephalopathy had biochemical abnormalities consistent with nonketotic hyperglycinemia. Cranial CT showed agenesis of the corpus callosum, gyral malformation, and ventricular enlargement. Similar brain abnormalities occurred in 9 of 15 previously reported patients. Including this patient, agenesis of the corpus callosum appeared in 6 of 15 patients, gyral malformation in 6 of 14, ventricular enlargement in 5 of 15, and cerebellar hypoplasia in 2 of 16. Nonketotic hyperglycinemia thus joins a growing list of inborn errors of metabolism associated with brain malformations.
一名出现肌阵挛性脑病的2周龄婴儿,其生化异常与非酮症高甘氨酸血症相符。头颅CT显示胼胝体发育不全、脑回畸形和脑室扩大。在先前报道的15例患者中,有9例出现了类似的脑部异常。包括该患者在内,15例患者中有6例出现胼胝体发育不全,14例中有6例出现脑回畸形,15例中有5例出现脑室扩大,16例中有2例出现小脑发育不全。因此,非酮症高甘氨酸血症加入了与脑畸形相关的先天性代谢缺陷的不断增加的名单中。