Incidence of chromosomal anomalies in fetuses with isolated right aortic arch: A meta‐analysis

2019 ◽  
Vol 40 (3) ◽  
pp. 294-300
Author(s):  
Qingyi Luo ◽  
Jian Chen ◽  
Yu Zhang ◽  
Jianhua Li ◽  
Xuan Su ◽  
...  
Keyword(s):  
Aortic Arch ◽  
Meta Analysis ◽  
Right Aortic Arch ◽  
Chromosomal Anomalies

scholarly journals Fetuses with right aortic arch: a multicenter cohort study and meta-analysis

2016 ◽  
Vol 47 (4) ◽  
pp. 423-432 ◽  
Author(s):  
F. D'Antonio ◽  
A. Khalil ◽  
V. Zidere ◽  
J. S. Carvalho
Keyword(s):  
Cohort Study ◽  
Aortic Arch ◽  
Meta Analysis ◽  
Right Aortic Arch ◽  
Multicenter Cohort Study ◽  
Multicenter Cohort

scholarly journals Postnatal Outcome and Associated Anomalies of Prenatally Diagnosed Right Aortic Arch with Concomitant Right Ductal Arch: A Systematic Review and Meta-Analysis

Diagnostics ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 831
Author(s):  
Paolo Ivo Cavoretto ◽  
Alexandros Sotiriadis ◽  
Serena Girardelli ◽  
Silvia Spinillo ◽  
Massimo Candiani ◽  
...  
Keyword(s):  
Systematic Review ◽  
Quality Assessment ◽  
Aortic Arch ◽  
Assessment Tool ◽  
Chromosomal Abnormalities ◽  
Meta Analysis ◽  
Random Effect ◽  
Random Effect Model ◽  
Case Series ◽  
Right Aortic Arch

Right aortic arch presents a reported incidence of 0.1% of the general population; the aim of our study was to evaluate the risk of associated intracardiac (ICA), extracardiac (ECA), or chromosomal abnormalities in fetuses with right aortic arch (RAA) and concomitant right ductal arch (RDA). A systematic review of the literature selected 18 studies including 60 cases of RAA/RDA. A meta-analysis with a random effect model calculated for each outcome the pooled crude proportion of associated abnormal outcomes in cases of RAA/RDA and the pooled proportions and odds ratios in RAA with LDA or RDA. Quality assessment of the included studies was achieved using the NIH quality assessment tool for case series studies. RAA/RDA presents risk of associated conotruncal CHDs of about 30% and risk of 22q11 microdeletion in the region of 1%. Two-thirds of 22q11 microdeletions had concomitant thymic hypoplasia and no other chromosomal defects were described. Risks for ICA, ECA, 22q11 microdeletion, and aberrant left subclavian artery are not substantially different in RAA with right or left arterial duct. RAA increases the risk of associated cardiac defects regardless of laterality of the ductal arch. In isolated RDA/RAA cases, absolute risks of extracardiac associated problems or surgery are rather low, we would therefore recommend reassurance, particularly when the thymus and karyotype are normal.

Characteristics of prenatally detected right aortic arch cases in a single institution

2018 ◽  
Vol 38 (7) ◽  
pp. 895-898 ◽  
Author(s):  
Melih Velipasaoglu ◽  
Metin Sentürk ◽  
Reyhan Ayaz ◽  
Barbaros Atesli ◽  
H. Mete Tanir
Keyword(s):  
Aortic Arch ◽  
Right Aortic Arch ◽  
Single Institution

scholarly journals Resection of Kommerell’s diverticulum in an infant with prenatal diagnosis of right aortic arch

2019 ◽  
Vol 5 (1) ◽  
Author(s):  
Kenji Suzuki ◽  
Takashi Sasaki ◽  
Shinobu Kunugi ◽  
Yoshio Shima ◽  
Ryuji Fukazawa ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Aortic Arch ◽  
Right Aortic Arch ◽  
Kommerell’S Diverticulum
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