scholarly journals Prenatal diagnosis of aberrant right subclavian artery in an unselected population

2017 ◽  
Vol 36 (3) ◽  
pp. 278-283 ◽  
Author(s):  
Mi Jin Song ◽  
Byoung Hee Han ◽  
Young-Hwa Kim ◽  
So Young Yoon ◽  
Yoo Mi Lee ◽  
...  
2020 ◽  
Vol 47 (1) ◽  
pp. 359-367
Author(s):  
Cristina Martínez‐Payo ◽  
Elena Suanzes ◽  
Yolanda Nieto‐Jiménez ◽  
Miguel Ruiz de Azúa ◽  
Ana Siles ◽  
...  

2014 ◽  
Vol 22 (1) ◽  
pp. 61-63
Author(s):  
Özge Kızılkale ◽  
Canan Yılmaz Torun ◽  
Mert Yeşiladalı ◽  
Pınar Cenksoy ◽  
Gazi Yıldırım ◽  
...  

Author(s):  
Cátia Sofia Ferreira Pinto Lourenço ◽  
Ana Luísa Carriço ◽  
Francisco Manuel da Silva Valente

Abstract Objective The objective of the present study was to determine the frequency of malformations and chromosomal abnormalities in a population of fetuses with an aberrant right subclavian artery (ARSA). Methods This is a 6-year retrospective study of fetuses with a prenatal diagnosis of ARSA conducted during the period between September 2013 and June 2019 at a fetal medicine unit. Data were collected from ultrasound, fetal echocardiograms, genetic studies, and neonatal records. Results An ARSA was diagnosed in 22 fetuses. An ARSA was an isolated finding in 18 out of 22 cases (82%). Associated abnormal sonographic findings were found in 4 cases. All cases underwent invasive testing. In 1 of the cases, a chromosomal abnormality was detected (mos 45,X [13]/46,X,e(X) (p22.1q22.1)). No cases of congenital heart disease were found in any of these fetuses. There were two cases in which the postnatal evaluation revealed a malformation: one case of hypospadias and 1 case of cleft palate. Conclusion The presence of an isolated ARSA is benign and is not associated with chromosomal abnormalities. The finding of ARSA, however, warrants a detailed fetal ultrasound in order to exclude major fetal abnormalities and other soft markers.


Author(s):  
M.V. Medvedev, N.A. Altynnik, A.I. Zamiatina et all

Six cases of prenatal ultrasound diagnosis of aberrant right subclavian artery at 12+2–14+2 weeks of gestation are presented. To 5 cases earlier published was added a case of prenatal diagnosis of the right aberrant subclavian artery in fetus with multiple congenital abnormalities at 13+3 weeks of gestation. Opportunities of early prenatal ultrasound diagnosis of the right aberrant subclavian artery on first screening are discussed.


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