Observation versus prophylactic Ladd procedure for asymptomatic intestinal rotational abnormalities in heterotaxy syndrome: A systematic review-Reference-Cited by-同舟云学术

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Observation versus prophylactic Ladd procedure for asymptomatic intestinal rotational abnormalities in heterotaxy syndrome: A systematic review

Published:2015-11 Issue:11 Volume:50 Page:1971-1974
ISSN:0022-3468
Container-title:Journal of Pediatric Surgery
language:en
Short-container-title:Journal of Pediatric Surgery

Author:

Landisch Rachel,Abdel-Hafeez Abdel-Hafeez,Massoumi Roxanne,Christensen Melissa,Shillingford Amanda,Wagner Amy J.

Publisher

Elsevier BV

Subject

General Medicine,Pediatrics, Perinatology and Child Health,Surgery

Reference18 articles.

1. Ladd's procedure in functional single ventricle and heterotaxy syndrome: does timing affect outcome?;Sharma;Ann Thorac Surg,2013

2. Heterotaxia syndromes and their abdominal manifestations;Borenstein;Curr Opin Pediatr,2006

3. Heterotaxy syndrome: is a prophylactic Ladd procedure necessary in asymptomatic patients?;Pockett;Pediatr Cardiol,2013

4. Congenital heart disease and heterotaxy: upper gastrointestinal fluoroscopy can be misleading and surgery in an asymptomatic patient is not beneficial;Papillon;J Pediatr Surg,2013

5. Heterotaxy syndrome and malrotation: does isomerism influence risk and decision to treat;Hill;J Pediatr Surg,2014

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Heterotaxy Syndrome Diagnosed in an Adult;Ochsner Journal;2024-08-22

2. Outcomes After Ladd Procedures for Intestinal Malrotation in Newborns with Heterotaxy Syndrome;Journal of Pediatric Surgery;2023-06

3. Malrotation and Fibroblast Growth Factor Receptor-2–Associated Craniosynostosis: An Underrecognized Association and Management Pathway;Journal of Craniofacial Surgery;2022-11-18

4. Neonatal Congenital Heart Disease Surgical Readiness and Timing;Pediatrics;2022-11-01

5. A multi-disciplinary, comprehensive approach to management of children with heterotaxy;Orphanet Journal of Rare Diseases;2022-09-09

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