Medium Chain Acyl CoA Dehydrogenase Deficiency and Eating Disorders: An Underreported Coincidence
Author:
Affiliation:
1. Royal Perth Hospital, Australia; University of Western Australia, Australia
2. Royal Perth Hospital, Australia
3. Royal Perth Hospital, Australia; University of Western Australia, Australia; Fiona Stanley Hospital Network, Australia
Publisher
FapUNIFESP (SciELO)
Link
http://www.scielo.br/scielo.php?script=sci_pdf&pid=S2326-45942024000100501&tlng=en
Reference33 articles.
1. Medium-chain Acyl-COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment;Mason E;Endocrinol Diabetes Metab,2023
2. The clinical manifestation of MCAD deficiency: Challenges towards adulthood in the screened population;Schatz UA;J Inherit Metab Dis,2010
3. Neonatal screening for medium chain acyl-CoA deficiency: High incidence in Lower Saxony (northern Germany);Sander S;Eur J Pediatr,2001
4. Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency,2024
5. Management and diagnosis of mitochondrial fatty acid oxidation disorders: Focus on very-long-chain acyl-CoA dehydrogenase deficiency;Yamada K;J Hum Genet,2019
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