A Young Female With Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD): A Case Report

Author:

Yusuf Ibidapo Q,Venkatesan Aadithiyavikram,Okafor Faith C,Yasin Athar,Oyibo Samson O

Publisher

Springer Science and Business Media LLC

Subject

Aerospace Engineering

Reference11 articles.

1. The portal for rare diseases and orphan drugs (Orphanet). Medium chain acyl-CoA dehydrogenase deficiency. (2014). Accessed. February 20, 2023: https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=42.

2. Medium-chain acyl-coenzyme A dehydrogenase deficiency;Merritt JL 2nd,2023

3. British Inherited Metabolic Disease Group (BIMDG). Adult emergency management. medium chain fat oxidation disorders. (2018). Accessed: February 20, 2023: https://www.bimdg.org.uk/store/guidelines/ADULT_MCAD-rev_2015_566641_09012016.pdf.

4. The clinical manifestation of MCAD deficiency: challenges towards adulthood in the screened population;Schatz UA;J Inherit Metab Dis,2010

5. Adult-onset very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD);Fatehi F;Eur J Neurol,2020

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