Prenatal diagnosis of Marfan syndrome by fetal echocardiography: A case report and review of cardiovascular manifestations-Reference-Cited by-同舟云学术

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Prenatal diagnosis of Marfan syndrome by fetal echocardiography: A case report and review of cardiovascular manifestations

Published:2019-12-27 Issue:2 Volume:37 Page:359-362
ISSN:0742-2822
Container-title:Echocardiography
language:en
Short-container-title:Echocardiography

Author:

Wang Xin¹²^ORCID,Sun Lin¹²,Liu Xiao‐Wei¹²,Shang Jian‐Feng³,He Yi‐Hua¹²^ORCID

Affiliation:

1. Department 2 of Echocardiography Beijing Anzhen Hospital Capital Medical University Beijing China

2. Fetal Heart Disease Maternal Fetal Medicine Research Important Laboratories Beijing China

3. Pathology department of Beijing Anzhen Hospital Capital Medical University Beijing China

Funder

Beijing Municipal Science & Technology Commission

National Key R&D Program of China

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine,Radiology Nuclear Medicine and imaging

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/echo.14577

Reference7 articles.

1. Fetal Cardiac Manifestations of Marfan Syndrome

2. Fetal marfan syndrome: Prenatal ultrasound diagnosis with pathological confirmation of skeletal and aortic lesions

3. Prenatal diagnosis of neonatal Marfan syndrome

4. Neonatal Marfan syndrome diagnosed prenatally

5. Development of Z -scores for fetal cardiac dimensions from echocardiography

Cited by 4 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. Current status and challenges in prenatal and neonatal screening, diagnosis, and management of congenital heart disease in China;The Lancet Child & Adolescent Health;2023-07

2. Early-onset Marfan syndrome with a novel missense mutation: A case report;Journal of Cardiology Cases;2023-06

3. Prenatal ultrasound diagnosis of primary myxomatous degeneration of cardiac valves in a fetus: Case report;Journal of Obstetrics and Gynaecology Research;2022-07-10

4. Functional Analysis of an Intronic FBN1 Pathogenic Gene Variant in a Family With Marfan Syndrome;Frontiers in Genetics;2022-04-25

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