References
Carpenter KH, Bonham JR, Clarke A (1990) Rett's syndrome and ornithine carbamoyltransferase deficiency.J Inher Metab Dis 13: 308–310.
Naidu S, Moser HW (1990) Peroxisomal disorders.Neurol Clin 8: 507–528.
Robinson BH, MacMillan H, Petrova-Benedict R, Sherwood WG (1987) Variable clinical presentation in patients with deficiency E1 component of pyruvate dehydrogenase complex.J Pediatr 111: 525–533.
Willems PJ, Dijkstra I, Schierbeek HH, Berger R, Smit GPA (1988) Activation of fatty acid oxidation in the Silver-Russell syndrome and the Brachmann-de Lange syndrome.Am J Med Genet 30: 865–873.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Cazgan, A.L., Parano, E., Pavone, L. et al. Metabolic dysfunction in Russell-Silver syndrome. J Inherit Metab Dis 17, 244–245 (1994). https://doi.org/10.1007/BF00711627
Issue Date:
DOI: https://doi.org/10.1007/BF00711627