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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
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...
Autores principales: | Hartung, Benno, Tank, Anne, Dittmann, Sven, Ritz-Timme, Stefanie, Schulze-Bahr, Eric |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
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 |
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