Journal of Inherited Metabolic Disease

, Volume 10, Issue 1, pp 95–96 | Cite as

Lethal multiple acyl-CoA dehydrogenation deficiency with dysmorphic features

  • M. J. Bennett
  • R. J. Pollitt
  • J. M. Land
  • M. J. Turner
  • C. H. Cheetham
Case Report

Keywords

Public Health Internal Medicine Metabolic Disease Dysmorphic Feature 

References

  1. Boue, J., Chalmers, R. A., Tracey, B. M., Watson, D., Gray, R. G. F., Keeling, J. W., King, G. S., Pettit, B. R., Lindenbaum, R. H., Rocchiccioli, F. and Saudubray, J-M. Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduria.Lancet 1 (1984) 846–847Google Scholar
  2. Goodman, S. I., Reale, M. and Barlow, S. Glutaric acidemia type II: A form with deleterious intrauterine effects.J. Pediatr. 102 (1983) 411–413Google Scholar
  3. Lehnert, W., Wendel, V., Lindenmeier, S. and Bohn, N. Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. 1. Clinical, metabolic and biochemical findings.Eur. J. Pediatr. 139 (1982) 60–64Google Scholar
  4. Sweetman, L., Nyhan, W. L., Trauner, D. A., Merritt, T. A. and Singh, M. Glutaric aciduria type II.J. Pediatr. 96 (1980) 1020–1026Google Scholar

Copyright information

© SSIEM and MTP Press Limited 1987

Authors and Affiliations

  • M. J. Bennett
    • 1
  • R. J. Pollitt
    • 2
  • J. M. Land
    • 3
  • M. J. Turner
    • 3
  • C. H. Cheetham
    • 4
  1. 1.Department of Chemical PathologyThe Children's HospitalSheffieldUK
  2. 2.MRC External Scientific Staff, Neonatal Screening Laboratory and University Department of PsychiatryMiddlewood HospitalSheffieldUK
  3. 3.Department of PathologyWycombe General HospitalBucks.UK
  4. 4.Department of PaediatricsWycombe General HospitalHigh WycombeUK

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