Case report: Prenatal diagnosis of fetal non-compaction cardiomyopathy with bradycardia accompanied by de novo CALM2 mutation

We herein report what appears to be the first case of fetal non-compaction cardiomyopathy in both ventricles accompanied by a mutation in the calmodulin gene (CALM2). A 25-year-old woman was referred to our hospital at 25(+1) weeks of gestation for evaluation of fetal defects. Prenatal echocardiogra...

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Detalles Bibliográficos
Autores principales: Zhang, Wen, Dai, Xiaohui, Liu, Hanmin, Li, Lei, Zhou, Shu, Zhu, Qi, Chen, Jiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727144/
https://www.ncbi.nlm.nih.gov/pubmed/36507129
http://dx.doi.org/10.3389/fped.2022.1012600

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727144/
https://www.ncbi.nlm.nih.gov/pubmed/36507129
http://dx.doi.org/10.3389/fped.2022.1012600

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