Faculty Opinions recommendation of Fetal aortic valve stenosis and the evolution of hypoplastic left heart syndrome: patient selection for fetal intervention.

Author(s):  
Larry Latson
Circulation ◽  
2006 ◽  
Vol 113 (11) ◽  
pp. 1401-1405 ◽  
Author(s):  
Kaarin Mäkikallio ◽  
Doff B. McElhinney ◽  
Jami C. Levine ◽  
Gerald R. Marx ◽  
Steven D. Colan ◽  
...  

2019 ◽  
Vol 09 (02) ◽  
pp. e121-e126
Author(s):  
Amna Qasim ◽  
Chelsea Johnson ◽  
Muhammad Aly ◽  
Ashraf Aly

Introduction Congenital absence of the aortic valve leaflets is a rare association with hypoplastic left heart syndrome (HLHS). Case A 37-year-old pregnant woman was referred for fetal evaluation of possible HLHS at 22 weeks of gestation. The fetal echocardiogram (ECHO) was remarkable for a hypoplastic left atrium, nearly atretic mitral valve, small left ventricle, and a hypoplastic aortic valve with severe aortic insufficiency. A female infant was born at term and postnatal ECHO confirmed the above findings. In addition, there was complete absence of the aortic valve leaflets. The patient underwent Norwood's procedure at day 5 of life with atrial septectomy, over-sewing of the aortic valve annulus, and a 4 mm Sano's shunt between the right ventricle and the main pulmonary artery. She tolerated this surgery well and subsequently underwent a bidirectional Glenn's procedure at 8 months of life. Conclusion Prenatal diagnosis of absent aortic valve should be suspected in the presence of severe aortic insufficiency in the fetal ECHO. Early postnatal intervention is critical as those patients are likely to deteriorate quickly. The over-sewing of the aortic valve may be important to prevent coronary steal and myocardial hypoperfusion which could potentially be detrimental.


2004 ◽  
Vol 128 (2) ◽  
pp. 315-316 ◽  
Author(s):  
Narutoshi Hibino ◽  
Yorikazu Harada ◽  
Takeshi Hiramatsu ◽  
Satoshi Yasukochi ◽  
Gengi Satomi

2018 ◽  
Vol 34 (1) ◽  
pp. 3-9
Author(s):  
Hirofumi Fukunaga ◽  
Makoto Nakamura ◽  
Shiro Ishikawa ◽  
Yoshihiko Kodama ◽  
Koichi Sagawa ◽  
...  

2015 ◽  
Vol 26 (3) ◽  
pp. 599-601
Author(s):  
Gopalan Nair Rajesh ◽  
Sandeep Mohanan ◽  
Haridasan Vellani

AbstractMitral atresia is commonly seen as a part of the spectrum of hypoplastic left heart syndrome, and it is usually associated with multiple levels of systemic outflow tract obstruction. Isolated mitral atresia with a normal aortic valve is extremely rare. We report the rare combination of mitral atresia, transposition of the great arteries, and unobstructed systemic and pulmonary blood flow.


2021 ◽  
Vol 37 (2) ◽  
pp. 185-192
Author(s):  
Emily Hildebrand

Hypoplastic left heart syndrome (HLHS) comprises a spectrum of left-sided heart anomalies resulting from left outflow or inflow obstruction. Obstruction most often occurs at the levels of the aortic valve and/or mitral valve due to stenosis or atresia. HLHS is a lethal cardiac anomaly if not treated within the first week of life. Knowledge of sonographic features could aid in early detection, which results in better planning and management of pregnancy. This report presents a case in which HLHS was discovered during a routine dating and viability sonogram, performed at 12 weeks’ gestation.


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