| Literature DB >> 10945697 |
A Cheikhelard1, P De Lagausie, C Garel, J Maintenant, E Vuillard, P Blot, Y Aigrain.
Abstract
The authors report 3 different cases of prenatal diagnosis of situs inversus associated with bowel malrotation. Heterotaxy existed in 2 cardiosplenic syndromes (1 left and 1 right isomerism), and 1 isolated situs inversus. Bowel malrotation was detected at birth by ultrasonography and intestinal contrast study. Patients underwent laparoscopic LADD's procedure and abdominal exploration in the neonatal period. The authors advocate neonatal screening and early surgical management of bowel malrotation in prenatally diagnosed heterotaxic syndromes.Entities:
Mesh:
Year: 2000 PMID: 10945697 DOI: 10.1053/jpsu.2000.8730
Source DB: PubMed Journal: J Pediatr Surg ISSN: 0022-3468 Impact factor: 2.545