Literature DB >> 27844411

Fetal Situs, Isomerism, Heterotaxy Syndrome: Diagnostic Evaluation and Implication for Postnatal Management.

Karl Degenhardt1,2, Jack Rychik3,4.   

Abstract

OPINION STATEMENT: A hallmark of vertebrate anatomy is asymmetry of structures, especially internal organs, on the left and right side of the body. Heterotaxy syndrome is the combination of correct-sided, and incorrect-sided organs. The establishment of the left-right axis is an early event in vertebrate embryogenesis. Failure to establish this axis has numerous consequences for later development and can result in a wide range of potential defects. Congenital heart disease is among the more frequent and serious problems. Heterotaxy syndrome is diagnosed prenatally with increasing frequency due to improved screening practices. The key to proper management of fetal heterotaxy syndrome is reliable determination of left and right in the fetus, a thorough understanding of associated defects and comprehensive imaging.

Entities:  

Keywords:  Congenital heart disease; Heterotaxy syndrome; Pediatrics; Vertebrate embryogenesis

Year:  2016        PMID: 27844411     DOI: 10.1007/s11936-016-0494-2

Source DB:  PubMed          Journal:  Curr Treat Options Cardiovasc Med        ISSN: 1092-8464


  42 in total

Review 1.  Observation versus prophylactic Ladd procedure for asymptomatic intestinal rotational abnormalities in heterotaxy syndrome: A systematic review.

Authors:  Rachel Landisch; Abdel-Hafeez Abdel-Hafeez; Roxanne Massoumi; Melissa Christensen; Amanda Shillingford; Amy J Wagner
Journal:  J Pediatr Surg       Date:  2015-08-08       Impact factor: 2.545

2.  Outcome of high-risk neonates with congenital complete heart block paced in the first 24 hours after birth.

Authors:  Andrew C Glatz; J William Gaynor; Larry A Rhodes; Jack Rychik; Ronn E Tanel; Victoria L Vetter; Jonathan R Kaltman; Susan C Nicolson; Lisa Montenegro; Maully J Shah
Journal:  J Thorac Cardiovasc Surg       Date:  2008-06-12       Impact factor: 5.209

3.  Congenital complete heart block in the fetus: hemodynamic features, antenatal treatment, and outcome in six cases.

Authors:  M Eronen; P Heikkilä; K Teramo
Journal:  Pediatr Cardiol       Date:  2001 Sep-Oct       Impact factor: 1.655

4.  Situs anomalies on prenatal MRI.

Authors:  Stefan F Nemec; Peter C Brugger; Ursula Nemec; Dieter Bettelheim; Gregor Kasprian; Gabriele Amann; David L Rimoin; John M Graham; Daniela Prayer
Journal:  Eur J Radiol       Date:  2011-06-28       Impact factor: 3.528

5.  High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.

Authors:  Nader Nakhleh; Richard Francis; Rachel A Giese; Xin Tian; You Li; Maimoona A Zariwala; Hisato Yagi; Omar Khalifa; Safina Kureshi; Bishwanath Chatterjee; Steven L Sabol; Matthew Swisher; Patricia S Connelly; Mathew P Daniels; Ashok Srinivasan; Karen Kuehl; Nadav Kravitz; Kimberlie Burns; Iman Sami; Heymut Omran; Michael Barmada; Kenneth Olivier; Kunal K Chawla; Margaret Leigh; Richard Jonas; Michael Knowles; Linda Leatherbury; Cecilia W Lo
Journal:  Circulation       Date:  2012-04-12       Impact factor: 29.690

6.  Recessively inherited right atrial isomerism caused by mutations in growth/differentiation factor 1 (GDF1).

Authors:  Eevi Kaasinen; Kristiina Aittomäki; Marianne Eronen; Pia Vahteristo; Auli Karhu; Jukka-Pekka Mecklin; Eero Kajantie; Lauri A Aaltonen; Rainer Lehtonen
Journal:  Hum Mol Genet       Date:  2010-04-22       Impact factor: 6.150

7.  Diabetes mellitus and birth defects.

Authors:  Adolfo Correa; Suzanne M Gilboa; Lilah M Besser; Lorenzo D Botto; Cynthia A Moore; Charlotte A Hobbs; Mario A Cleves; Tiffany J Riehle-Colarusso; D Kim Waller; E Albert Reece
Journal:  Am J Obstet Gynecol       Date:  2008-07-31       Impact factor: 8.661

8.  When the right (Drug) should be left: Prenatal drug exposure and heterotaxy syndrome.

Authors:  Nicole R van Veenendaal; Cynthia D J Kusters; Roelof-Jan Oostra; Jorieke E H Bergman; Jan-Maarten Cobben
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2016-03-15

9.  Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.

Authors:  Erich Roessler; Maia V Ouspenskaia; Jayaprakash D Karkera; Jorge I Vélez; Amy Kantipong; Felicitas Lacbawan; Peter Bowers; John W Belmont; Jeffrey A Towbin; Elizabeth Goldmuntz; Benjamin Feldman; Maximilian Muenke
Journal:  Am J Hum Genet       Date:  2008-06-05       Impact factor: 11.025

10.  Association between maternal chronic conditions and congenital heart defects: a population-based cohort study.

Authors:  Shiliang Liu; K S Joseph; Sarka Lisonkova; Jocelyn Rouleau; Michiel Van den Hof; Reg Sauve; Michael S Kramer
Journal:  Circulation       Date:  2013-06-28       Impact factor: 29.690

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  2 in total

1.  Successful Palliation via Kawashima Procedure of an Infant With Heterotaxy Syndrome and Left-Atrial Isomerism.

Authors:  Hannah Lively-Endicott; Diego A Lara
Journal:  Ochsner J       Date:  2018

2.  Heterotaxy syndrome with intestinal malrotation, polysplenia and azygos continuity.

Authors:  Stéphanie Cupers; Christine Van Linthout; Brigitte Desprechins; Léon Rausin; Martine Demarche; Marie-Christine Seghaye
Journal:  Clin Pract       Date:  2018-01-08
  2 in total

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