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Updated: Apr 17, 2026

Quantification of Coenzyme A in Cells and Tissues
Published on: September 27, 2019
Successful management of pregnancy with very-long-chain acyl-coenzyme A dehydrogenase deficiency
Hiroko Yamamoto1, Daisuke Tachibana1, Go Tajima2
1Department of Obstetrics and Gynecology, Osaka City University Graduate School of Medicine, Osaka, Japan.
Abstract:
Very-long-chain acyl-coenzyme A dehydrogenase deficiency (VLCADD) is a rare and life-threatening disease characterized by an enzymatic defect in the fatty acid β-oxidation pathway. A nulliparous woman with VLCADD showed improvements in serum levels of the long-chain acylcarnitine moiety (C14:1) during pregnancy and successfully delivered a healthy infant vaginally. Pregnancy and vaginal delivery can be successfully completed in patients with VLCADD with careful management.
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