Results 231 to 240 of about 2,246,280 (273)
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The Challenge of Pediatric Heart Transplantation in a Failing Fontan Patient With Dextrocardia and Heterotaxy Syndrome.

World journal for pediatric & congenital heart surgery
Patients with dextrocardia, heterotaxy syndrome, and single ventricle physiology typically undergo multiple staged palliative operations culminating in a Fontan circulation.
H. Sicim   +4 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   +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   +5 more
semanticscholar   +1 more source

Evaluation of a Case with Biliary Atresia and Heterotaxy Syndrome (Left Isomerism) in Terms of Liver Transplantation: A Case Report

Journal of Inonu Liver Transplantation Institute
im-Left isomerism, a subtype of heterotaxy marked by multiple spleens and abnormal organ ...
Huseyin Ayvaz
semanticscholar   +1 more source

Intra-abdominal haemorrhaging after cardiac catheterisation: the importance of recognising vascular anomalies in heterotaxy syndrome

Cardiology in the Young, 2023
A 2-month-old boy with a single ventricle underwent cardiac catheterisation. Inferior vena cava angiography at the end of the examination revealed local stenosis, flexion, and connection to the right hepatic vein. Six hours after catheterisation, he went
Yuya Yamada, Y. Ishikawa, Koichi Sagawa
semanticscholar   +1 more source

Heterotaxy Syndrome with Esophageal Atresia

The Journal of Pediatrics, 2015
newborn presented with a prenatal diagnosis of hy-dramnios, dysplastic kidney, and congenital heart dis-ease and suspected heterotaxy syndrome. His 38-week gestation was complicated by maternal cholestasis. Anamniocentesiswasperformedandkaryotypewas46,XY.Thirdtrimesterserologieswerenegativeandthemotherwasimmuneto rubella and not immune to toxoplasmosis.
Filipa, Flor-de-Lima   +6 more
openaire   +2 more sources

Intrauterine diagnosis of heterotaxy syndrome

American Heart Journal, 2002
Heterotaxy syndrome, including right isomerism and left isomerism, is characterized by an abnormal symmetry of the viscera and veins and is frequently associated with complex cardiac anomalies. We sought to define the feasibility of in utero diagnosis and the postnatal outcome.Patients with heterotaxy syndrome were identified from 579 fetal ...
Jiuann-Huey, Lin   +7 more
openaire   +2 more sources

Fetale Heterotaxie-Syndrome

Der Gynäkologe, 2006
Das mit den Heterotaxie-Syndromen assoziierte Spektrum von Fehlbildungen umfasst eine Vielzahl von kardiovaskularen und viszeralen Anomalien, die mit unterschiedlicher Haufigkeit bei den beiden Hauptvarianten Rechts-Isomerismus und Links-Isomerismus auftreten und sowohl den intrauterinen als auch den postnatalen Verlauf entscheidend beeinflussen. Daher
C. Berg, U. Gembruch, A. Geipel
openaire   +1 more source

Molecular genetics of heterotaxy syndromes

Current Opinion in Cardiology, 2004
Heterotaxy is a complex set of birth defects in which the normal concordance of asymmetric thoracic and abdominal organs is disturbed. In this review the authors summarize recent research on the etiology of heterotaxy syndromes. Improved understanding of the genetic control of left-right patterning in the early embryo is leading to the identification ...
John W, Belmont   +3 more
openaire   +2 more sources

Virtual reality modelling for planning of percutaneous first step palliation in a newborn with heterotaxy syndrome

Cardiology in the Young
We report the first-stage percutaneous palliation in a newborn with a rare heterotaxy syndrome variant including interrupted inferior vena cava, partial anomalous pulmonary venous drainage, and restrictive interatrial communication.
Aleksandra Dziewulska   +2 more
semanticscholar   +1 more source

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