Technical principles of computed tomography in patients with congenital heart disease [PDF]
, 2011 Cardiac magnetic resonance imaging and echocardiography are often the primary imaging techniques for many patients with congenital heart disease (CHD). However, with modern generations of CT systems and recent advances in temporal and spatial resolution,
Bjoern Stinn +6 more
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Unusual association of polysplenia syndrome with abdominal teratoma
Journal of Indian Association of Pediatric Surgeons, 2011 Report of a hitherto unreported association of polysplenia, teratoma and eventration of diaphragm.
Kushaljit Singh Sodhi +5 more
doaj +1 more source
Unusual, unexpected course of temporary pacing lead leading to diagnosis of a rare syndrome
IHJ Cardiovascular Case Reports, 2019 We describe a case of an elderly female with complete heart block where temporary pacemaker insertion led to diagnosis of inferior vena cava interruption, leading further to diagnosis of polysplenia syndrome.
M.P. Girish +4 more
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Ivemark syndrome: asplenia with kidney collecting duct cysts and polysplenia with cerebellar cyst
The Turkish Journal of Pediatrics, 2000 Two newborns, one male and one female, from two different families, with Ivemark syndrome proven at autopsy are reported. One of them had asplenia and another had polysplenia.
V Krźelj +5 more
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Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia [PDF]
, 2010 Generalised lymphatic dysplasia (GLD) is characterised by extensive peripheral lymphoedema with visceral involvement. In some cases, it presents in utero with hydrops fetalis. Autosomal dominant and recessive inheritance has been reported.
Brice, G +11 more
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Aid decision algorithms to estimate the risk in congenital heart surgery [PDF]
, 2016 Background and objective: In this paper, we have tested the suitability of using different artificial intelligence-based algorithms for decision support when classifying the risk of congenital heart surgery.
Marin-Alonso, Oscar +4 more
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Diagnóstico imagenológico en el Síndrome de Abernethy [PDF]
, 2017 El shunt portosistémico congénito (SPSC) o Síndrome de Abernethy es una patología muy poco frecuente, descrita por primera vez en 1793 por John Abernethy.
Bufaliza, Jorge +4 more
core
De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations [PDF]
, 2015 BACKGROUND: Genomic disorders resulting from deletion or duplication of genomic segments are known to be an important cause of cardiovascular malformations (CVMs).
Austin, E. +18 more
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Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia [PDF]
, 2016 OBJECTIVES: To prospectively assess the value of serum total bilirubin (TB) within 3 months of hepatoportoenterostomy (HPE) in infants with biliary atresia as a biomarker predictive of clinical sequelae of liver disease in the first 2 years of life ...
Arnon, Ronen +23 more
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Congenital lobar emphysema associated with polysplenia syndrome
Annals of Saudi Medicine, 2010 Polysplenia, or left isomerism, is a rare heterotaxy syndrome characterized by bilateral bi-lobed lungs, bilateral pulmonary atria, a symmetrical midline liver, and multiple aberrant splenic nodules.
Choh Naseer +3 more
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