Summary
A child with propionic acidaemia, after a stormy infantile course complicated by microcephaly, has shown normal subsequent growth and development without dietary protein restriction.
Similar content being viewed by others
References
Bain, M. D., Borriello, S. P., Tracey, B. M., Jones, M., Reed, P. J., Chalmers, R. A. and Stacey, T. E. Contribution of gut bacterial metabolism to human metabolic disease.Lancet 1 (1988) 1078–1079
Brandt, I. K., Hsia, Y. E., Clement, D. H. and Provence, S. A. Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development.Pediatrics 53 (1974) 391–395
Elsas, L. J. and Acosta, P. B. Nutritional support of inherited metabolic diseases. In Shils, M. E. and Young, V. R. (eds.)Modern Nutrition in Health and Disease, edn. 7, Lea and Febiger, Philadelphia, 1988, pp. 1337–1379
Harris, D. J., Yang, B. I., Thompson, R. M. and Wolf, B. Propionyl CoA carboxylase deficiency presenting as non-ketotic hyperglycinemia.J. Med. Genet. 18 (1981) 156–157
Ledley, F. D., Levy, H. L., Shih, V. E., Benjamin, R. and Mahoney, M. J. Benign methylmalonic aciduria.N. Engl. J. Med. 311 (1984) 1015–1018
Walter, J. H., Thompson, G. N., Leonard, J. V.et al. Propionate and protein turnover in methylmalonic and propionic acidemia. Abstracts of the25th SSIEM Annual Symposium, London, SSIEM, 1987
Waterlow, J. C., Garlick, P. J. and Millward, D. J.Protein Turnover in Mammalian Tissues and in the Whole Body, North Holland, Amsterdam, 1978
Wolf, B., Paulsen, E. P. and Hsia, Y. E. Asymptomatic propionyl CoA carboxylase deficiency in a 13-year-old girl.J. Pediatr. 95 (1979) 563–565
Yannicelli, S. Nutritional support of methylmalonic acidemia.Ross Metabolic Currents, Ross Laboratories, Columbus, Ohio. 1 (1988) 10–13
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Luder, A.S., Yannicelli, S. & Green, C.L. Normal growth and development with unrestricted protein intake after severe infantile propionic acidaemia. J Inherit Metab Dis 12, 307–311 (1989). https://doi.org/10.1007/BF01799222
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF01799222