Molecular and clinical characteristics of very long-chain acyl-CoA dehydrogenase deficiency: A single-center experience in Saudi Arabia

Amal Alhashem; Sarar Mohamed; Manal Abdelraheem; Bushra AlGufaydi; Aida Al-Aqeel

doi:10.15537/smj.2020.6.25131

Article Information

vol. 41 no. 6 590-596

DOI

https://doi.org/10.15537/smj.2020.6.25131

PubMed

32518924

Published By

Saudi Medical Journal

Online ISSN

1658-3175

History

Received April 7, 2020
Accepted May 20, 2020
Published online June 1, 2020.

Copyright: © Saudi Medical Journal This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Author Information

Amal Alhashem, MD, FMG,
Sarar Mohamed, FRCPCH, MD ⇑,
Manal Abdelraheem, MD, MRCPCH,
Bushra AlGufaydi, MD, ABP and
Aida Al-Aqeel, FRCP, FACMG

From the Department of Pediatrics (Alhashem, Abdelrahim, AlGufaydi, Al-Aqeel, Mohamed), Prince Sultan Military Medical City; from the Department of Pediatrics (Alhashem, Mohamed); from the Department of Anatomy and Embryology (Al-Aqeel), College of Medicine, AlFaisal University; from Prince Abdullah bin Khalid Celiac Disease Research Chair (Mohamed), King Saud University, Riyadh, Kingdom of Saudi Arabia; and from the Department of Biochemistry and Molecular Biology (Al-Aqeel), College of Medicine, American University of Beirut, Beirut, Lebanon.

Address correspondence and reprint request to: Dr. Sarar Mohamed, Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia. E-amil: [email protected] ORCID ID: https://orcid.org./0000-0002-7393-5064

View Full Text