Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1973 Dec;48(12):975–977. doi: 10.1136/adc.48.12.975

Child with a defect in leucine metabolism associated with beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria.

D Gompertz, K Bartlett, D Blair, C M Stern
PMCID: PMC1648668  PMID: 4765660

Full text

PDF
975

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Eldjarn L., Jellum E., Stokke O., Pande H., Waaler P. E. Beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria: a new inborn error of metabolism. Lancet. 1970 Sep 5;2(7671):521–522. doi: 10.1016/s0140-6736(70)90140-6. [DOI] [PubMed] [Google Scholar]
  2. Gompertz D., Draffan G. H. The gas-chromatographic diagnosis of intermittent maple syrup urine disease (branch-chain ketoaciduria). Clin Chim Acta. 1972 Aug;40(1):5–11. doi: 10.1016/0009-8981(72)90244-6. [DOI] [PubMed] [Google Scholar]
  3. Gompertz D., Draffan G. H. The identification of tiglylglycine in the urine of a child with -methylcrotonylglycinuria. Clin Chim Acta. 1972 Mar;37:405–410. doi: 10.1016/0009-8981(72)90462-7. [DOI] [PubMed] [Google Scholar]
  4. Gompertz D., Draffan G. H., Watts J. L., Hull D. Biotin-responsive beta-methylcrotonylglycinuria. Lancet. 1971 Jul 3;2(7714):22–24. doi: 10.1016/s0140-6736(71)90009-2. [DOI] [PubMed] [Google Scholar]
  5. Stokke O., Eldjarn L., Jellum E., Pande H., Waaler P. E. Beta-methylcrotonyl-CoA carboxylase deficiency: a new metabolic error in leucine degradation. Pediatrics. 1972 May;49(5):726–735. [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES