Results 81 to 90 of about 2,423 (197)

Unusual association of polysplenia syndrome with abdominal teratoma

open access: yesJournal 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

Technical principles of computed tomography in patients with congenital heart disease [PDF]

open access: yes, 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
core   +1 more source

De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations [PDF]

open access: yes, 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
core   +1 more source

Unusual, unexpected course of temporary pacing lead leading to diagnosis of a rare syndrome

open access: yesIHJ 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
doaj   +1 more source

Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia [PDF]

open access: yes, 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
core   +1 more source

Ivemark syndrome: asplenia with kidney collecting duct cysts and polysplenia with cerebellar cyst

open access: yesThe 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
doaj  

Diagnóstico imagenológico en el Síndrome de Abernethy [PDF]

open access: yes, 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  

Aid decision algorithms to estimate the risk in congenital heart surgery [PDF]

open access: yes, 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
core   +2 more sources

Preduodenal Portal Vein And Polysplenia: A Case Report and Review Of Literature [PDF]

open access: yes, 2022
Preduodenal portal vein (PDPV) is a rare anomaly in which the portal vein courses anterior to the second part of the duodenum. PDPV is often associated with other congenital anomalies such as polysplenia, malrotation and pancreatic anomalies.
Bamberger, P. Kurt   +3 more
core   +1 more source

CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes [PDF]

open access: yes, 2015
CHD is frequently associated with a genetic syndrome. These syndromes often present specific cardiovascular and non-cardiovascular co-morbidities that confer significant peri-operative risks affecting multiple organ systems.
Cooper, David S.   +2 more
core   +1 more source

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