Biochemical abnormalities in an infant with sudanophilic leukodystrophy
R. Sengers
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorJ. Bakkeren
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorW. Ruitenbeek
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorF. Trijbels
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorJ. Rotteveel
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorJ. Slooff
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorA. Janssen
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorR. Sengers
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorJ. Bakkeren
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorW. Ruitenbeek
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorF. Trijbels
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorJ. Rotteveel
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorJ. Slooff
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this authorA. Janssen
Departments of Paediatrics and Pathology, University of Nijmegen, P.O. Box 9101, Nijmegen, 6500 HB The Netherlands
Search for more papers by this author
References
- 1Cederbaum S. D., Blass J. P., Minkoff N., Brown W. J., Cotton M. E., Harris S. H. (1976) Sensitivity to carbohydrate in a patient with familial intermittent lactic acidosis and pyruvate dehydrogenase deficiency. Pediatr. Res., 10: 713–720.
- 2Hommes F. A., Polman H. A., Reerink J. D. (1968) Leigh's encephalomyelopathy: an inborn error of gluconeogenesis. Arch. Dis. Child., 43: 423–426.
- 3Saudubray J. M., Marsac C., Charpentier C., Cathelineau L., Besson Leaud M., Leroux J. P. (1976) Neonatal congenital lactic acidosis with pyruvate carboxylase deficiency in two siblings. Acta Paediatr. Scand., 65: 717–724.
- 4Sengers R. C. A., Krijgsman J. B., Trijbels J. M. F., Ruitenbeek W., Janssen A. J. M., Ter Laak H. J., Jaspar H. J. J., Stadhouders A. M., Busch H. F. M., Jenniskens F. G. I., Scholte H. R. (1981) Mitochondrial abnormalities, rod formation, muscle lipoamide dehydrogenase deficiency and dysmyelinisation. In: Mitochondria and Muscular Diseases, The Netherlands: Mefar, Beetsterzwaag, 191–198.
