Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report

BACKGROUND: Left ventricular noncompaction (LVNC) is a rare inherited cardiomyopathy with a broad phenotypic spectrum. The genotype-phenotype correlations in fetal-onset LVNC have not yet been fully elucidated. In this report, we present the first case of severe fetal-onset LVNC caused by maternal l...

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Detalles Bibliográficos
Autores principales: Kawamura, Hiroshi, Ikawa, Masamichi, Hirono, Keiichi, Kimura, Junya, Okuno, Takashi, Kawatani, Masao, Inai, Kunihiro, Hata, Yukiko, Nishida, Naoki, Yoshida, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285293/
https://www.ncbi.nlm.nih.gov/pubmed/37360367
http://dx.doi.org/10.3389/fped.2023.1195222

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285293/
https://www.ncbi.nlm.nih.gov/pubmed/37360367
http://dx.doi.org/10.3389/fped.2023.1195222

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