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Whither heterotaxy?

Published online by Cambridge University Press:  29 July 2021

Robert H. Anderson*
Affiliation:
Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK
Diane E. Spicer
Affiliation:
Congenital Heart Center, Department of Surgery and Pediatrics, University of Florida, Gainesville, FL, USA Heart Institute, Johns Hopkins All Children’s Hospital, Saint Petersburg, FL, USA
Rohit S. Loomba
Affiliation:
Heart Institute, Advocate Hospital, Oak Lawn, IL, USA
Justin T. Tretter
Affiliation:
Heart Institute, Cincinnati Children’s Hospital Medical Center, Department of Pediatrics, University of Cincinnati, College of Medicine, Cincinnati, OH, USA
*
Author for correspondence: Prof. R. H. Anderson, 60 Earlsfield Road, London SW18 3DN, UK. Tel: +00 44 20 8870 4368. E-mail: Sejjran@ucl.ac.uk

Abstract

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Type
Commentaries
Copyright
© The Author(s), 2021. Published by Cambridge University Press

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References

Moreau de Bellaing, A, Bonnet, D, Houyel, L. Abnormal origin of the left pulmonary artery from the descending aorta and heterotaxy syndrome: an undescribed phenotypic association. Cardiol Young. This issue.Google Scholar
Loomba, RS, Aiello, S, Tretter, JT, et al. Left pulmonary artery from the ascending aorta: a case report and review of published cases. J Cardiovasc Dev Dis 2021; 8: 1.Google Scholar
Franklin, RCG, Béland, MJ, Colan, SD, et al. Nomenclature for congenital and paediatric cardiac disease: the international paediatric and congenital cardiac code (IPCCC) and the eleventh iteration of the international classification of diseases (ICD-11). Cardiol Young 2017; 27: 18721938.CrossRefGoogle Scholar
Jacobs, JP, Anderson, RH, Weinberg, PM, et al. The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy. Cardiol Young 2007; 17 (Suppl 2): 128.Google ScholarPubMed
Anderson, RH, Spicer, DE, Loomba, RS. Is an appreciation of isomerism the key to unlocking the mysteries of the cardiac findings in heterotaxy? J Cardiovasc Dev Dis 2018; 5: 11.CrossRefGoogle ScholarPubMed
Anonymous. A general and particular History of Anomalies of Organization in Man and Animals, comprising Researches into the Characters, Classification, Sfc. of Monstrosities. By M. Isidore Geoffroy St. Hilaire, M.D., &C. &C. Paris, 1832–36. 3 Vols. 8vo, with an Atlas. Br Foreign Med Rev 1839; 1–39.Google Scholar
Uemura, H, Ho, SY, Devine, WA, et al. Atrial appendages and venoatrial connections in hearts from patients with visceral heterotaxy. Ann Thorac Surg 1995; 60: 561569.CrossRefGoogle ScholarPubMed
Tremblay, C, Loomba, RS, Frommelt, PC, et al. Segregating bodily isomerism or heterotaxy: potential echocardiographic correlations of morphological findings. Cardiol Young 2017; 27: 14701480.CrossRefGoogle ScholarPubMed
Anderson, C, Devine, WA, Anderson, RH, Debich, DE, Zuberbuhler, JR. Abnormalities of the spleen in relation to congenital malformations of the heart: a survey of necropsy findings in children. Br Heart J 1990; 63: 122128.CrossRefGoogle ScholarPubMed
The Gospel according to Saint Mark, Chapter 12, verse 17.Google Scholar
Van Praagh, S. Cardiac malpositions and the heterotaxy syndromes. In: Keane, JF, Lock, JE, Fyler, DC (eds). Nadas’ Pediatric Cardiology, 2nd edn. Elsevier, Philadelphia, PA, 2006: 675695.CrossRefGoogle Scholar
Van Praagh, R, David, I, Wright, GB, Van Praagh, S. Large RV plus small LV is not single LV. Circulation 1980; 61: 10571058.CrossRefGoogle Scholar
Loomba, RS, Pelech, AN, Shah, PH, Anderson, RH. Determining bronchial morphology for the purposes of segregating so-called heterotaxy. Cardiol Young 2016; 26: 725737.CrossRefGoogle ScholarPubMed