aortic arch interruption
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Medicine ◽  
2021 ◽  
Vol 100 (46) ◽  
pp. e27879
Author(s):  
WenSheng Zhang ◽  
WeiFang Xing ◽  
MinZhen Zhu ◽  
XiaoJing Zhong ◽  
JinZhao He


2021 ◽  
Vol 13 (4) ◽  
pp. 302
Author(s):  
Magalie Kaya ◽  
Paul Neville ◽  
Nathalie Soulé ◽  
Jacques Poinsot ◽  
Jean Marc El Arid ◽  
...  


Author(s):  
Rocío A. Peña-Juarez ◽  
Miguel A. Medina-Andrade ◽  
Carlos A. Corona-Villalobos ◽  
Juan P. Abarca-De la Paz


2020 ◽  
Vol 11 (4) ◽  
pp. 507-508
Author(s):  
Mrinal Patel ◽  
Vishal Agrawal ◽  
Vaibhav Jain ◽  
Bhavik Langanecha ◽  
Amit Mishra

Truncus arteriosus (TA) or common arterial trunk is a congenital cardiac anomaly having high association with arch anomalies such as right aortic arch or aortic arch interruption. However, TA with double aortic arch (DAA) is a rare occurrence. We report a case of TA with DAA where the diagnosis of DAA was missed initially.



2020 ◽  
Author(s):  


2020 ◽  
pp. 933-939
Author(s):  
Serban C. Stoica


Author(s):  
I.V. Komarova, A.A. Nikiforenko, E.F. Khmeleva et all

Two cases of prenatal diagnosis of a deletion syndrome 22q11.2 are presented. They are includes the cardiovascular defects in combination with hypoplasia of the thymus. In first case the pregnancy was aborted due to the heart disease, adverse for life (aortic arch interruption). In second case (right aorta arch and left aberrant subclavial artery) the pregnancy was prolonged, the chromosomal pathology was diagnosed at the age of 3 months. Modern data on clinic, diagnosis and outcome of a syndrome at the fetus, children and adults are analyzed. The possibility of the aim prenatal diagnosis of syndrome on the basis of the characteristic conotruncal abnormalities in combination with hypoplasia of thymus is presented.



Aorta ◽  
2019 ◽  
Vol 07 (03) ◽  
pp. 084-086
Author(s):  
Duccio Federici ◽  
Samuele Bichi ◽  
Gianfranco Montesi ◽  
David Matiashvili ◽  
Cristina Agostinis ◽  
...  

AbstractAortic coarctations in adults are mainly represented by recurrent critical narrowing at the site of previous surgical correction, or less frequently by native forms of complex obstructive malformations of the distal arch and isthmus. We present our experience with an unusual form of native adult aortic coarctation presenting as a complete interruption of the aortic arch.



2019 ◽  
Vol 27 (7) ◽  
pp. 590-592
Author(s):  
Joaquín Pérez-Andreu ◽  
Joaquín Fernández-Doblas ◽  
Gemma Giralt García ◽  
Ferran Roses ◽  
Raúl F Abella

The case of a newborn with a post-ductal interrupted aortic arch combined with severe hypoplasia of the thoracic descending aorta and intracardiac defects is described. Extraanatomic bypass surgery was performed in the neonatal period to connect the ascending and descending parts of the aorta. Closure of a ventricular septal defect and excision of hypertrophied bands in the right ventricle with subsequent ventriculotomy were delayed beyond neonatal age.



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