You briefly explain MCAD deficiency to the parents, emphasizing that you do not yet know whether the infant has MCAD deficiency. However, until it has been ruled out, it is important that the parents ...

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a genetically inherited disorder that compromises the mitochondrial breakdown of medium-chain fatty acids. This metabolic impairment can lead ...

N.B. Please note that if you are outside North America the embargo for Lancet Press material is 0001 hours Uk time Friday 28 Septemner 2001. Results of a study in this week’s issue of THE LANCET ...

HOUSTON - Researchers at The University of Texas MD Anderson Cancer Center have discovered a novel function for the metabolic enzyme medium-chain acyl-CoA dehydrogenase (MCAD) in glioblastoma (GBM).

You receive a phone call from the state screening laboratory about one of your patients, a 9-day-old infant boy born at 39 weeks of gestation by normal vaginal delivery with an Apgar score of 9/9. He ...