Fatal multiple acyl-CoA dehydrogenase deficiency caused by ETFDH gene mutation: A case report

This is the authors' abstract. We don't add key points for this paper.

Multiple acyl-CoA dehydrogenase deficiency (MADD) is a disease of rare autosomal recessive disorder. There are three types of MADD. Type I is a neonatal-onset form with congenital anomalies. Type II is a neonatal-onset form without congenital anomalies. Type III is considered to a milder form and usually responds to riboflavin. However, late-onset form could also be fatal and not responsive to treatments.