Nowaczyk M J, Blaser S I, Clarke J T
Department of Pediatrics, Hospital for Sick Children, University of Toronto, Ontario, Canada.
Am J Med Genet. 1998 Jan 23;75(3):292-6.
Central nervous system malformations have been reported in a number of inherited enzyme defects. Ethylmalonic encephalopathy, an organic aciduria of unknown pathogenesis, has not been reported previously in association with brain or spinal cord malformations. We report on 2 sibs with confirmed ethylmalonic encephalopathy and malformations of the central nervous system; one with tethered cord, the other with cerebellar tonsillar ectopia (Chiari I malformation).
中枢神经系统畸形已在多种遗传性酶缺陷中被报道。乙基丙二酸脑病是一种发病机制不明的有机酸尿症,此前尚未有与脑或脊髓畸形相关的报道。我们报告了2例确诊为乙基丙二酸脑病且伴有中枢神经系统畸形的同胞;1例患有脊髓栓系,另1例患有小脑扁桃体下疝(Chiari I畸形)。