References
Cowan, M. J., Wara, D. W., Packman, S., Ammann, A. J., Yoshino, M., Sweetnam, L. and Nyhan, W. Multiple biotin-dependent carboxylase deficiencies associated with defects in T-cell and B-cell immunity.Lancet 2 (1979) 115–118
Munnich, A., Saudubray, J. M., Cotisson, A., Coude, F. X., Ogier, H., Charpentier, C., Marsac, C., Carre, G., Bourgeay-Causse, M. and Frezal, J. Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosis.Eur. J. Pediatr. 137 (1981) 203–206
Swick, H. M. and Kien, C. L. Biotin deficiency with neurologic and cutaneous manifestations but without organic aciduria.J. Pediatr. 103 (1983) 265–267
Van Biervliet, J. P. G. M., Bruinvis, L., Van der Heiden, C., Ketting, D., Wadman, S. K., Willemse, J. L. and Monnens, L. A. H. Report of a patient with severe chronic lactic acidaemia and pyruvate carboxylase deficiency.Devl. Med. Child Neurol. 19 (1977) 392–401
Wolf, B., Grier, R. E., Allen, R. J., Goodman, S. I. and Kien, C. L. Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency.Clin. Chim. Acta 131 (1983a) 273–278
Wolf, B., Grier, R. E., Allen, R. J., Goodman, S. I., Kien, C. L., Parker, W. D., Howell, D. M. and Hurst, D. L. Phenotypic variation in biotinidase deficiency.J. Pediatr. 103 (1983b) 233–237
Wolf, B., Grier, R. E., Parker, W. D., Goodman, S. I. and Allen, R. J. Deficient biotinidase activity in late-onset multiple carboxylase deficiency.N. Engl. J. Med. 308 (1983c) 161
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Erasmus, C., Mienie, L.J., Reinecke, C.J. et al. Organic aciduria in late-onset biotin-responsive multiple carboxylase deficiency. J Inherit Metab Dis 8 (Suppl 2), 105–106 (1985). https://doi.org/10.1007/BF01811480
Issue Date:
DOI: https://doi.org/10.1007/BF01811480