Published in Volume
50, Issue 1
(January 1971)J Clin Invest.
1971, The American Society for
Inherited propionyl-CoA carboxylase deficiency in “ketotic hyperglycinemia”
Division of Medical Genetics, Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut 06510
Division of Medical Genetics, Department of Medicine, Yale University School of Medicine, New Haven, Connecticut 06510
Published January 1971
Cultured fibroblasts from a young girl with ketotic hyperglycinemia were unable to oxidize propionate-14C to 14CO2, but oxidized methylmalonate-14C and succinate-14C normally. This block in propionate catabolism was shown to result from a lack of propionyl-CoA carboxylase activity. The carboxylase deficiency was not due to the presence of an intracellular inhibitor and it was not corrected by biotin, a known cofactor for the enzyme. Both of her parents' fibroblasts had approximately 50% of normal propionyl-CoA carboxylase activity. These results demonstrate that ketotic hyperglycinemia and propionicacidemia are the same disease, caused by a mutation of the propionyl-CoA carboxylase apoenzyme, which is inherited as an autosomal recessive trait. This enzymatic localization provides an explanation for the remarkable clinical and chemical similarity between ketotic hyperglycinemia and methylmalonicaciduria and offers a potential means of antenatal detection of this disorder.
Click on an image below to see the page. View
PDF of the complete article