Does a combination of ultrasound, MRI, and biochemical amniotic fluid analysis improve prenatal diagnosis of esophageal atresia?

Author:

Garabedian C.1,Verpillat P.2,Czerkiewicz I.3,Langlois C.4,Muller F.3,Avni F.2,Bigot J.2,Sfeir R.5,Vaast P.1,Coulon C.1,Subtil D.16,Houfflin-Debarge V.16

Affiliation:

1. Department of Obstetrics; Jeanne de Flandre Hospital, CHRU de Lille; Lille France

2. Department of Pediatric Radiology; Jeanne de Flandre Hospital, CHRU de Lille; Lille France

3. Biochemistry-Hormonology Department, Robert Debré Hospital, AP-HP; University Paris Ile de France Ouest; Paris France

4. Department of Biostatistics, EA2694, UDSL; University of Lille Nord de France, CHRU de Lille; Lille France

5. Reference Center for Congenital Esophageal Abnormalities (CRACMO); Lille France

6. University of Lille Nord de France; Lille France

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference19 articles.

1. Epidemiology of esophageal atresia;Sfeir;Dis Esophagus,2013

2. Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions;Pedersen;Arch Dis Child,2012

3. Oesophageal atresia;Spitz;Orphanet J Rare Dis,2007

4. Esophageal obstruction-prenatal detection rate and outcome;Brantberg;Ultrasound Obstet Gynecol,2007

5. Prenatal diagnosis of esophageal atresia with the pouch sign;Centini;Ultrasound Obstet Gynecol,2003

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