Annals of Pediatric Cardiology
About us | Current Issue | Archives | Ahead of Print | Instructions | Submission | Subscribe | Advertise | Contact | Login 
Read this article


    Article Cited by others


Non-cardiac issues in patients with heterotaxy syndrome

Kothari Shyam S

Year : 2014| Volume: 7| Issue : 3 | Page no: 187-192

   This article has been cited by
1 Situs Deconstructed
William N. Evans
Pediatric Cardiology. 2022;
[Pubmed]  [Google Scholar] [DOI]
2 Cholangitis secondary to obstructive choledocholithiases in an elderly woman with heterotaxy syndrome with polysplenia: report of a case and brief review of the literature
Antonio Jesús Láinez Ramos-Bossini, Paula Córdoba-Peláez, Pablo Redruello-Guerrero
Clinical Journal of Gastroenterology. 2022;
[Pubmed]  [Google Scholar] [DOI]
3 Whole genome sequencing in transposition of the great arteries and associations with clinically relevant heart, brain and laterality genes
Gillian M. Blue, Mauk Mekel, Debjani Das, Michael Troup, Emma Rath, Eddie Ip, Mikhail Gudkov, Gopinath Perumal, Richard P. Harvey, Gary F. Sholler, Jozef Gecz, Edwin P. Kirk, Jinfen Liu, Eleni Giannoulatou, Haifa Hong, Sally L. Dunwoodie, David S. Winlaw
American Heart Journal. 2022; 244: 1
[Pubmed]  [Google Scholar] [DOI]
4 A multi-disciplinary, comprehensive approach to management of children with heterotaxy
Thomas G. Saba, Gabrielle C. Geddes, Stephanie M. Ware, David N. Schidlow, Pedro J. del Nido, Nathan S. Rubalcava, Samir K. Gadepalli, Terri Stillwell, Anne Griffiths, Laura M. Bennett Murphy, Andrew T. Barber, Margaret W. Leigh, Necia Sabin, Adam J. Shapiro
Orphanet Journal of Rare Diseases. 2022; 17(1)
[Pubmed]  [Google Scholar] [DOI]
5 Splenic Infarct with Polysplenia Syndrome
Qin Ling Zhu, wenjun zhu
Journal of the Belgian Society of Radiology. 2022; 106(1)
[Pubmed]  [Google Scholar] [DOI]
6 A Rare Case of Pulmonary Embolism in a Patient With Interrupted Inferior Vena Cava and Polysplenia
Mahmoud M Mansour, Omar Hussein, Baraa Saad, Alexander Shinn, Tarang Patel
Cureus. 2022;
[Pubmed]  [Google Scholar] [DOI]
7 Incidental Finding of Heterotaxy Syndrome in a Patient With Pulmonary Embolism: A Case Report and Concise Review
Mohamed Mahmoud, Khadija El Kortbi, Hayoung Wang, Joseph Wang
Cureus. 2022;
[Pubmed]  [Google Scholar] [DOI]
8 Heterotaxy Syndrome: Discordant Growth
Pratiksha Yadav, Pranav Ajmera, Sruthi Krishnamurthy , Nikhil B Nandivada
Cureus. 2021;
[Pubmed]  [Google Scholar] [DOI]
9 A Rare Case of Recurrent Pneumonia in Heterotaxy Syndrome, Polysplenia/Left Isomerism
Ayesha Anwar, Jacob Jubin, Shafi Raza, Zafar K Mirza
Cureus. 2021;
[Pubmed]  [Google Scholar] [DOI]
10 Putting two toes out of line… mirror-image accessory toes in female monozygotic twins
Deirdre J Foley, Brendan Paul Murphy
Archives of Disease in Childhood. 2021; 106(1): 30
[Pubmed]  [Google Scholar] [DOI]
11 Impact of Motile Ciliopathies on Human Development and Clinical Consequences in the Newborn
Rachael M. Hyland, Steven L. Brody
Cells. 2021; 11(1): 125
[Pubmed]  [Google Scholar] [DOI]
12 Cardiac Development: A Glimpse on Its Translational Contributions
Diego Franco, Carlos Garcia-Padilla, Jorge N. Dominguez, Estefania Lozano-Velasco, Amelia Aranega
Hearts. 2021; 2(1): 87
[Pubmed]  [Google Scholar] [DOI]
13 Splenic torsion in the setting of polysplenia syndrome
Margaret Kennedy, Daniel Farinas Lugo, William Raleigh Thompson
Journal of Pediatric Surgery Case Reports. 2021; 75: 102070
[Pubmed]  [Google Scholar] [DOI]
14 Heterotaxy polysplenia syndrome in an adult female with complete endocardial cushion defect
Habib Ahmad Esmat, Mohammad Wali Naseri, Asadullah Shirzai
Radiology Case Reports. 2021; 16(5): 1080
[Pubmed]  [Google Scholar] [DOI]
15 The multisystem nature of isomerism: left isomerism complicated by Abernethy malformation and portopulmonary hypertension
Megan L. Ringle, Rohit Loomba, John C. Dykes, Danyal Khan, David Schidlow, Gil Wernovsky
Cardiology in the Young. 2021; 31(4): 532
[Pubmed]  [Google Scholar] [DOI]
16 Prenatal and Neonatal Detection of Isomeric Situs and the Association with Maternal Comorbidities
William N. Evans, Ruben J. Acherman, Humberto Restrepo
Journal of Fetal Medicine. 2021;
[Pubmed]  [Google Scholar] [DOI]
17 Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding
Sanjeev Kharel, Dinesh Prasad Koirala, Suraj Shrestha, Hari Sedai, Bibek Man Shrestha, Sushan Homagain, Suraj Kandel
Clinical Case Reports. 2021; 9(8)
[Pubmed]  [Google Scholar] [DOI]
18 Fatal pneumococcal septicemia in a girl with visceral heterotaxy and polysplenia: a case report
Ingo von Both, Michael S. Pollanen
Forensic Science, Medicine and Pathology. 2020; 16(3): 519
[Pubmed]  [Google Scholar] [DOI]
19 Heterotaxy Is Not a Risk Factor for Adverse Long-Term Outcomes After Fontan Completion
Supreet P. Marathe, Diana Zannino, Jacob Y. Cao, Karin du Plessis, Shilpa S. Marathe, Julian Ayer, David S. Celermajer, Thomas L. Gentles, Gary F. Sholler, Robert N. Justo, Nelson Alphonso, Yves d’Udekem, David S. Winlaw
The Annals of Thoracic Surgery. 2020; 110(2): 646
[Pubmed]  [Google Scholar] [DOI]
20 Prenatal diagnosis of asplenia syndrome with sliding hiatus hernia in a fetus
Balaganesh Karmegaraj, SatjeetKaur Deol, Vivek Krishnan, Balu Vaidyanathan
Annals of Pediatric Cardiology. 2020; 13(2): 167
[Pubmed]  [Google Scholar] [DOI]
21 The twists and turns of left-right asymmetric gut morphogenesis
Julia Grzymkowski, Brent Wyatt, Nanette Nascone-Yoder
Development. 2020; 147(19)
[Pubmed]  [Google Scholar] [DOI]
22 Abnormalities of Fetal Situs
Tashima E. Lambert,Jeffrey Kuller,Maria Small,Eleanor Rhee,Piers Barker
Obstetrical & Gynecological Survey. 2016; 71(1): 33
[Pubmed]  [Google Scholar] [DOI]
23 Racial disparities in heterotaxy syndrome
Keila N. Lopez,Lisa K. Marengo,Mark A. Canfield,John W. Belmont,Heather A. Dickerson
Birth Defects Research Part A: Clinical and Molecular Teratology. 2015; 103(11): 941
[Pubmed]  [Google Scholar] [DOI]