Results 311 to 320 of about 8,530 (370)

Situs Inversus Totalis: A Case Report and Literature Review. [PDF]

Clin Case Rep
Du X, Wang N, Sheng J, Zhang Y, Gao J.
europepmc   +1 more source

Surgical management of hiatal hernia in a 3-year-old child with asplenia syndrome, congenital heart disease, thoracic scoliosis, and intestinal malrotation: A case report. [PDF]

Int J Surg Case Rep
Alhariri AM, Sleiay M, Zwaraa HN, Alqreea M, Abdulkader M, Brnbow ZM.   +5 more
europepmc   +1 more source

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Surgical Management of the Neonate With Heterotaxy and Long-Term Outcomes of Heterotaxy

World Journal for Pediatric & Congenital Heart Surgery, 2011
A review of the many challenges facing the neonate with heterotaxy has identified total anomalous pulmonary venous connection, atrioventricular valve abnormalities, pulmonary atresia, and arrhythmias including heart block as particular risk factors for the child who will pursue a single-ventricle pathway.
Richard A Jonas
exaly   +3 more sources

Outcomes after Ladd Procedures for Intestinal Malrotation in Newborns with Heterotaxy Syndrome.

Journal of Pediatric Surgery, 2023
PURPOSE Intestinal malrotation may be asymptomatic in patients with heterotaxy syndrome (HS), and whether these newborns benefit from prophylactic Ladd procedures is unknown.
C. T. Huerta, R. Saberi, R. Lynn, Walter A. Ramsey, G. Gilna, J. Parreco, J. Sola, E. Perez, C. Thorson   +8 more
semanticscholar   +1 more source

Long-term outcomes of functional single ventricles associated with heterotaxy syndrome.

European Journal of Cardio-Thoracic Surgery, 2023
OBJECTIVES The current study aimed to determine the long-term surgical outcomes of patients with functional single ventricles associated with heterotaxy syndrome, risk factors for mortality, and factors associated with Fontan stage completion.
Kazuki Tanimoto, Takaya Hoash, Keisuke Shibagaki, Yoshikazu Ono, Motoki Komori, Naoki Okuda, Kenta Imai, Shigemitsu Iwai, Hajime Ichikawa   +8 more
semanticscholar   +1 more source

Asymptomatic COVID-19 Reinfection in a Pediatric Patient with Heterotaxy Syndrome

Viral immunology, 2023
We report an asymptomatic child with heterotaxy syndrome who had recurrent positive SARS-CoV-2 polymerase chain reaction testing. An aberrant lymphocyte population expressing CD19, CD16, and CD56 was identified; its phenotyping revealing atypical NK ...
G. Erdem, C. Cua, A. Basu, Simon Lee, A. Leber, R. Abraham   +5 more
semanticscholar   +1 more source

The Conduction System in Heterotaxy

World Journal for Pediatric and Congenital Heart Surgery, 2011
Cardiac malformations associated with the syndrome of atriovisceral heterotaxy are among the most complex forms of congenital heart disease. Accordingly, the disposition of the specialized conduction tissue (the conduction system) is also variable and complex in these particular anomalies.
Hiromi, Kurosawa, Noriyasu, Kawada
openaire   +2 more sources

Heterotaxy syndrome: Prenatal diagnosis, concomitant malformations and outcomes

Prenatal Diagnosis, 2022
The aim of this study is to define cardiac and extracardiac malformations in fetuses with heterotaxy syndrome and to determine perinatal and childhood prognosis.
Munip Akalın, O. Demirci, P. Kumru, I. Yücel   +3 more
semanticscholar   +1 more source

Outcomes of Biventricular and Single Ventricle Heterotaxy Patients: A Single Center 5-Decade Experience.

Annals of Thoracic Surgery, 2022
BACKGROUND Surgical palliation of patients with heterotaxy syndrome has proven challenging. Long-term outcomes have historically been poor. Factors contributing to these outcomes are not completely understood.
Gabriel Graham, J. Dearani, T. Niaz, Sheri S. Crow, F. Cetta, E. Stephens   +5 more
semanticscholar   +1 more source