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A novel mutation in ACADVL causing very long-chain acyl-coenzyme-A dehydrogenase deficiency in a South Asian pediatric patient: a case report and review of the literature

Crossref DOI link: https://doi.org/10.1186/s13256-021-03013-y

Published Online: 2021-09-01

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Arunath, Visvalingam https://orcid.org/0000-0002-7705-0394
Liyanarachchi, Manoj Sanjeewa

Gajealan, Sundararajah

Jasinge, Eresha

Weerasekara, Kumudu

Moheb, Lia Abbasi
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Text and Data Mining valid from 2021-09-01

Version of Record valid from 2021-09-01
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Article History

Received: 7 August 2020

Accepted: 13 July 2021

First Online: 1 September 2021

Declarations

:

: Written informed consent was obtained from the patient’s parents for publication of this case report and the publication of genetic mutational analysis of the child.

: Written informed consent was obtained from the patient’s parents for publication of this case report. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

: The authors declare that they have no competing interests.

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