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

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

BackgroundLeft 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 low...

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Bibliographic Details
Main Authors: Hiroshi Kawamura, Masamichi Ikawa, Keiichi Hirono, Junya Kimura, Takashi Okuno, Masao Kawatani, Kunihiro Inai, Yukiko Hata, Naoki Nishida, Yoshio Yoshida
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-06-01
Series:Frontiers in Pediatrics
Subjects:
left ventricular noncompaction
myosin heavy chain 7
next-generation sequencing
mosaicism mutation
case report
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2023.1195222/full

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