Fetal Echocardiography is Useful for Screening Fetuses with a Family History of Cardiomyopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00246-020-02439-3.pdf
Reference29 articles.
1. van Spaendonck-Zwarts KY, van Rijsingen IA, van den Berg MP et al (2013) Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience. Eur J Heart Fail 15:628–636. https://doi.org/10.1093/eurjhf/hft013
2. Pedra SR, Hornberger LK, Leal SM, Taylor GP, Smallhorn JF (2005) Cardiac function assessment in patients with family history of nonhypertrophic cardiomyopathy: a prenatal and postnatal study. Pediatr Cardiol 26:543–552. https://doi.org/10.1007/s00246-004-0688-3
3. Lipshultz SE, Sleeper LA, Towbin JA et al (2003) The incidence of pediatric cardiomyopathy in two regions of the United States. N Engl J Med 348:1647–1655. https://doi.org/10.1056/NEJMoa021715
4. Weber R, Kantor P, Chitayat D et al (2014) Spectrum and outcome of primary cardiomyopathies diagnosed during fetal life. JACC Heart Fail 2:403–411. https://doi.org/10.1016/j.jchf.2014.02.010
5. Sivasankaran S, Sharland GK, Simpson JM (2005) Dilated cardiomyopathy presenting during fetal life. Cardiol Young 15:409–416. https://doi.org/10.1017/S1047951105000855
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Spectrum and Outcome of Prenatally Diagnosed Fetal Primary Cardiomyopathies—A Twenty-Year Overview;Journal of Clinical Medicine;2023-06-28
2. Morphological and genetic causes of fetal cardiomyopathies;Clinical Genetics;2023-05-20
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