Associated anomalies and outcome of fetal aberrant right subclavian artery View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-01

AUTHORS

Ahmet Gul, Aytul Corbacioglu, Isil Turan Bakirci, Yavuz Ceylan

ABSTRACT

PURPOSE: To determine the frequency of aberrant right subclavian artery among the low-risk fetuses and to evaluate its association with chromosomal abnormalities and the other congenital heart diseases. METHODS: A total of 4,125 consecutive fetuses were examined for the presence of aberrant right subclavian artery that arises from the descending aorta distal to the left subclavian artery. RESULTS: Aberrant right subclavian artery was detected in 17 cases (0.4%). In nine cases it was an isolated finding. In four cases (23.5%) it was accompanied by another cardiac defect. Extracardiac malformations were present in three fetuses (17.6%). Among the 13 cases of aberrant right subclavian artery in which the karyotypes were known, one case presented with Down syndrome (7.6%). In this fetus, aberrant right subclavian artery was the only finding. CONCLUSION: These findings suggest that aberrant right subclavian may be an isolated finding in trisomy 21. The visualization of subclavian artery should be a part of fetal echocardiographic examination as it may be a valuable marker for Down syndrome. More... »

PAGES

27-30

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00404-011-1907-9

DOI

http://dx.doi.org/10.1007/s00404-011-1907-9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1030078528

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/21487731


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