Abstract
The G985A mutation represents about 90% of all medium-chain acyl-CoA dehydrogenase (MCAD) allele mutations that cause the clinical symptoms of MCAD deficiency. The prevalence of carriers varies between different European populations, with high frequencies in the northwestern part of Europe. To determine the prevalence of MCAD carriers with the G985A mutation in The Netherlands, we collected 6195 Guthrie cards of newborns. Mutation detection was performed with the polymerase chain reaction (PCR), in which a NcoI restriction site was created in the presence of a G985A mutation in the PCR product, followed by NcoI digestion, and gel electrophoresis. We detected a G985A carrier frequency of 1 in 59 (95% CI 1/50–1/73) in The Netherlands. The total prevalence of carriers was estimated to be 1 in 55 (95% CI 1/46– 1/68), based on a relative G985A frequency of 94% in The Netherlands.
Similar content being viewed by others
Author information
Authors and Affiliations
Additional information
Received: 18 December 1995 / Revised: 14 February 1996
Rights and permissions
About this article
Cite this article
de Vries, H., Niezen-Koning, K., Kliphuis, J. et al. Prevalence of carriers of the most common medium-chain acyl-CoA dehydrogenase (MCAD) deficiency mutation (G985A) in The Netherlands. Hum Genet 98, 1–2 (1996). https://doi.org/10.1007/s004390050149
Issue Date:
DOI: https://doi.org/10.1007/s004390050149