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A rare case of adult-onset vanishing white matter leukoencephalopathy with movement disorder, expressing homozygous EIF2B3 and PRKN pathogenic variants

Crossref DOI link: https://doi.org/10.1186/s12883-024-04018-y

Published Online: 2025-01-04

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

Authors

Douden, Bashar Kamal Ali

Abufara, Yazan Mohammad Abdullah

Aldrabeeh, Mahmood Fayez Ali

Tell, Naela Ramadan Mohammad

Abudaya, Ismail
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Text and Data Mining valid from 2025-01-04

Version of Record valid from 2025-01-04
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Article History

Received: 10 October 2024

Accepted: 31 December 2024

First Online: 4 January 2025

Declarations

:

: Ethics approval for this study was obtained from the ethics committee of Al-Quds University, and informed consent was provided by the patient involved.

: Written informed consent was obtained from the patient for publication of this case report.

: The authors declare no competing interests.

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