Prenatal diagnosis of hypoplastic left heart syndrome associated with Noonan Syndrome and de novo RAF1 mutation

2012 ◽  
Vol 32 (10) ◽  
pp. 1016-1018 ◽  
Author(s):  
Solveig Schulz ◽  
Rosemarie Fröber ◽  
Cornelia Kraus ◽  
Uwe Schneider
2006 ◽  
Vol 25 (2) ◽  
pp. 245-249 ◽  
Author(s):  
Chandrakant R. Patel ◽  
John R. Lane ◽  
Michael L. Spector ◽  
Philip C. Smith ◽  
David J. Waight

2015 ◽  
Vol 117 (suppl_1) ◽  
Author(s):  
Almudena Martinez Fernandez ◽  
Xing Li ◽  
Jeanne L Theis ◽  
Andre Terzic ◽  
Timothy M Olson ◽  
...  

Hypoplastic Left Heart Syndrome (HLHS) is a complex multifactorial disease for which no definitive genetic causes have been found. Current genetic filtering strategies render lists of genes with unknown relevance in terms of pathogenesis. A complementary filter based on biological evidence would create a new approach to prioritize relevant candidate genes and mutations. In our study, 5 members of a nuclear family including a child with HLHS were evaluated using echocardiography and their genetic information was obtained through whole genome sequencing (WGS). Data filtering including rarity, functional impact and mode of inheritance was implemented, resulting in identification of 34 genes with recessive or de novo variants potentially involved in the pathogenesis of HLHS. Additionally, iPSC were derived from proband and parents and subjected to RNA-sequencing at the undifferentiated state and following spontaneous differentiation. Comparative transcriptional analyses identified genes differentially expressed in proband samples at each stage. These gene sets were used as an additional filter for the previously generated WGS data. This strategy revealed that out of 34 mutated genes originally identified, 10 displayed transcriptional differences in undifferentiated iPSC from the HLHS-affected individual while 16 out of 34 mutated genes showed significantly different expression levels in differentiated cells from proband. Furthermore, expression dynamics were studied during guided cardiac differentiation for the 9 genes fulfilling all applied criteria. Two genes not previously linked to HLHS, ELF4 and HSPG2 were found to behave significantly different in HLHS-iPSC when compared to control counterparts. In summary, filtering WGS data according to a new layer of transcriptional information that leverages iPSC plasticity allows prioritization of genes associated with HLHS in an in vitro model of disease.


1987 ◽  
Vol 6 (5) ◽  
pp. 261-264 ◽  
Author(s):  
R N Vincent ◽  
S Menticoglou ◽  
D Chanas ◽  
F Manning ◽  
G F Collins ◽  
...  

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.


2018 ◽  
Vol 218 (1) ◽  
pp. S290
Author(s):  
Kimberley A. Bullard ◽  
Brian L. Shaffer ◽  
Karen J. Scrivner ◽  
Rita Sharshiner ◽  
Maria I. Rodriguez ◽  
...  

2011 ◽  
Vol 108 (3) ◽  
pp. 421-427 ◽  
Author(s):  
Alaina K. Kipps ◽  
Colin Feuille ◽  
Anthony Azakie ◽  
Julien I.E. Hoffman ◽  
Sarah Tabbutt ◽  
...  

Herz ◽  
2003 ◽  
Vol 28 (3) ◽  
pp. 250-256 ◽  
Author(s):  
Paul M. Verheijen ◽  
Lukas A. Lisowski ◽  
Rutger F. Plantinga ◽  
J. Fran�ois Hitchcock ◽  
Ger B.W.E. Bennink ◽  
...  

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