Postmortem diagnosis of very long chain acyl‐CoA dehydrogenase (VLCAD) deficiency in a neonate with sudden cardiac death

Postmortem diagnosis of very long chain acyl‐CoA dehydrogenase (VLCAD) deficiency in a neonate with sudden cardiac death

Abstract Very long chain acyl‐CoA dehydrogenase (VLCAD) deficiency is an autosomal recessive long chain fatty acid β‐oxidation disorder with a variable clinical spectrum, ranging from an acute neonatal presentation with cardiac and hepatic failure to childhood or adult onset of symptoms with hepatom...

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Bibliographic Details
Main Authors: Prapti Singh, Deirdre Amaro, Olugbemisola Obi, FNU Kiran, Erin Hediger, Tomi L. Toler, Patricia I. Dickson, Dorothy K. Grange
Format: Article
Language:English
Published: Wiley 2023-07-01
Series:JIMD Reports
Subjects:
cardiac arrest
newborn screening
very long chain acyl CoA dehydrogenase (VLCAD) deficiency
Online Access:https://doi.org/10.1002/jmd2.12365

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