Literature DB >> 18008313

Population-based analysis of left- and right-sided diaphragmatic hernias demonstrates different frequencies of selected additional anomalies.

Anne M Slavotinek1, Barbara Warmerdam, Angela E Lin, Gary M Shaw.   

Abstract

Congenital diaphragmatic hernia (CDH) is a common birth defect that can be subdivided into several different types depending on the anatomical structures affected. Several studies have demonstrated that right-sided CDH (R-CDH) and left-sided CDH (L-CDH) in humans are associated with different clinical presentations and outcomes. We hypothesized that R-CDH and L-CDH are phenotypically and pathogenically distinct, and that the frequency of associated anomalies would differ among patients with R-CDH compared to patients with L-CDH. Using population-based data from ongoing studies in the California Birth Defects Monitoring Program (CBDMP), we compared 146 CDH cases, 38 with R-CDH (26%) and 108 with L-CDH (74%). The frequencies of atrial septal defect (1/38 R-CDH and 20/108 L-CDH cases; P = 0.015), bilateral pulmonary hypoplasia (22/108 L-CDH cases and 15/38 R-CDH cases; P = 0.029), abnormal skull or facial shape (17/108 L-CDH patients and 1/38 R-CDH cases; P = 0.043), assorted digital anomalies excluding syndactyly, polydactyly or absence of a digit (13/108 L-CDH patients and 0/38 R-CDH patients; P = 0.021) and assorted limb anomalies excluding limb reduction defects (18/108 L-CDH patients and 0.38 R-CDH patients; P = 0.004) all showed a statistically significant difference in frequency between R- and L-CDH patients. This descriptive epidemiological study using newborn surveillance data represents the largest comparison of right and left-sided CDH patients so far performed. Several anomalies as listed above were noted to be different in frequency between R- and L-CDH patients, although the interpretation of the significant variability in the frequency of these anomalies is not yet established and the findings require replication. Birth defects monitoring programs can provide the interface for epidemiology and clinical genetics, which in this case, may generate hypotheses to establish the pathogenesis of CDH laterality. (c) 2007 Wiley-Liss, Inc. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 18008313     DOI: 10.1002/ajmg.a.32100

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  6 in total

1.  Congenital Right Morgagni Hernia Presenting in an Adult-a Case Report.

Authors:  Sastha Ahanatha Pillai; Santhanakrishnan Chinnappan
Journal:  Indian J Surg       Date:  2015-11-13       Impact factor: 0.656

2.  Rare case report - congenital diaphragmatic hernia presentation in adult.

Authors:  Ajay Gujar; Dale Don Rodrigues; Kundan Patil; Uday Tambe; Shubha Sinha; Abhishek Bhushan
Journal:  Indian J Surg       Date:  2011-06-03       Impact factor: 0.656

Review 3.  Imaging of congenital diaphragmatic hernias.

Authors:  George A Taylor; Omolola M Atalabi; Judy A Estroff
Journal:  Pediatr Radiol       Date:  2008-07-08

4.  Laparoscopic cholecystectomy in an adult with agenesis of right hemidiaphragm and limb reduction defects: First report in literature.

Authors:  Julide Sagiroglu; Ercument Tombalak; Sarenur Basaran Yilmaz; Fikret Balyemez; Tunc Eren; Orhan Alimoglu
Journal:  North Clin Istanb       Date:  2015-11-04

5.  De Novo Duplication of 11p15 Associated With Congenital Diaphragmatic Hernia.

Authors:  Gabriel C Dworschak; Hartmut Engels; Jessica Becker; Lukas Soellner; Thomas Eggermann; Florian Kipfmueller; Andreas Müller; Heiko Reutter; Martina Kreiß
Journal:  Front Pediatr       Date:  2018-04-25       Impact factor: 3.418

6.  Case series on anesthesia for video-assisted thoracoscopic surgery for congenital diaphragmatic hernia in children.

Authors:  Anurag Aggarwal; Rohit Lohani; Varun Suresh
Journal:  Anesth Essays Res       Date:  2016 Jan-Apr
  6 in total

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