The first three years of screening for medium chain acyl-CoA dehydrogenase deficiency (MCADD) by newborn screening ontario

• Main Authors: Fisher Lawrence (Author), Wilson Kumanan (Author), Potter Beth K (Author), Kennedy Shelley (Author), Geraghty Michael (Author), Milburn Jennifer (Author), Chakraborty Pranesh (Author)
• Format: Book
• Published: BMC, 2010-11-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Medium chain acyl-CoA dehydrogenase deficiency (MCADD) is a disorder of mitochondrial fatty acid oxidation and is one of the most common inborn errors of metabolism. Identification of MCADD via newborn screening permits the introduct...