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A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations

Crossref DOI link: https://doi.org/10.1186/s12872-021-01977-9

Published Online: 2021-04-13

Published Print: 2021-12

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

Authors

Hartung, Benno http://orcid.org/0000-0003-1975-3320
Tank, Anne

Dittmann, Sven

Ritz-Timme, Stefanie

Schulze-Bahr, Eric
Funding

Funding for this research was provided by:

Universitätsklinikum Düsseldorf. Anstalt öffentlichen Rechts
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Text and Data Mining valid from 2021-04-13

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Article History

Received: 16 November 2020

Accepted: 2 April 2021

First Online: 13 April 2021

Ethics approval and consent to participate

: The case report complies with the current German law.

: Written informed consent was obtained from each family member resp. legal guardian for publication of this case report and any accompanying images. An anonymised copy of the written consent is available for review by the editor of this journal.

: The authors declare to have no conflict of interest.

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