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

BACKGROUND: Autopsies regularly aim to clarify the cause of death; however, relatives may directly benefit from autopsy results in the setting of heritable traits (“mortui vivos docent”). CASE PRESENTATION: A case of a sudden unexpected cardiac death of a 5.5-months-old child is presented. Autopsy a...

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Detalles Bibliográficos
Autores principales: Hartung, Benno, Tank, Anne, Dittmann, Sven, Ritz-Timme, Stefanie, Schulze-Bahr, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045169/
https://www.ncbi.nlm.nih.gov/pubmed/33849460
http://dx.doi.org/10.1186/s12872-021-01977-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045169/
https://www.ncbi.nlm.nih.gov/pubmed/33849460
http://dx.doi.org/10.1186/s12872-021-01977-9

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