dc.contributor.author | Yuksel, Atıl | |
dc.contributor.author | Gul, Ahmet | |
dc.contributor.author | Esmer, Aytul Corbacioglu | |
dc.contributor.author | Has, Recep | |
dc.contributor.author | Dural, Ozlem | |
dc.contributor.author | DEMIROREN, Tanju | |
dc.contributor.author | Nehir, Asli | |
dc.contributor.author | Kalelioglu, Ibrahim | |
dc.date.accessioned | 2021-03-04T09:39:57Z | |
dc.date.available | 2021-03-04T09:39:57Z | |
dc.date.issued | 2013 | |
dc.identifier.citation | Esmer A. C. , Gul A., Nehir A., Yuksel A., Dural O., Kalelioglu I., Has R., DEMIROREN T., "Detection Rate of Trisomy 21 in Fetuses with Isolated and Non-Isolated Aberrant Right Subclavian Artery", FETAL DIAGNOSIS AND THERAPY, cilt.34, sa.3, ss.140-145, 2013 | |
dc.identifier.issn | 1015-3837 | |
dc.identifier.other | av_694e2536-df54-4c78-ad48-a5c5f35eedea | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/72973 | |
dc.identifier.uri | https://doi.org/10.1159/000354650 | |
dc.description.abstract | Objective: The purpose of this study was to determine the frequency of chromosomal anomalies among the fetuses with isolated and non-isolated aberrant right subclavian artery (ARSA), and to evaluate the sonographic findings associated with ARSA. Methods: This is a retrospective study conducted during the period between January 2008 and December 2012 at the maternal fetal medicine units of three different referral centers. Results: Among the 148 cases of ARSA, 98 were isolated and 50 were associated with cardiac anomalies, extracardiac malformations or soft markers. Trisomy 21 was the only chromosomal anomaly with a prevalence of 6.8% (10/148). The corresponding rate was 6.1% (6/98) and 8% (4/50) for isolated and non-isolated ARSA, respectively. Cardiac anomalies, extracardiac findings and soft markers were detected in 5.4% (8), 10.8% (16) and 24.3% (36) of cases, respectively. Among the 10 fetuses with trisonny 21, 6 were isolated, 4 were associated with soft markers, 2 were associated with fetal growth restriction and 1 was associated with hydrops fetalis. Cardiac anomalies were not observed in any of these fetuses. Conclusion: The prenatal diagnosis of ARSA should prompt meticulous anatomic survey, and karyotype analysis might be offered even in the absence of associated findings. Copyright (C) 2013 S. Karger AG, Basel | |
dc.language.iso | eng | |
dc.subject | Kadın Hastalıkları ve Doğum | |
dc.subject | Cerrahi Tıp Bilimleri | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | KADIN HASTALIKLARI & DOĞUM | |
dc.title | Detection Rate of Trisomy 21 in Fetuses with Isolated and Non-Isolated Aberrant Right Subclavian Artery | |
dc.type | Makale | |
dc.relation.journal | FETAL DIAGNOSIS AND THERAPY | |
dc.contributor.department | İstanbul Üniversitesi , , | |
dc.identifier.volume | 34 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 140 | |
dc.identifier.endpage | 145 | |
dc.contributor.firstauthorID | 4794 | |