Results 71 to 80 of about 2,404 (180)
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
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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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Preduodenal Portal Vein And Polysplenia: A Case Report and Review Of Literature [PDF]
, 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
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CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes [PDF]
, 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
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Situs Ambiguous with Polysplenia
Gazi Medical Journal, 2012 Situs ambiguous with polysplenia is a situs abnormality characterized by the duplication of left-sided organs and presence of multiple spleens. Situs anomalies are rare conditions with a developmental origin where the inner organs are located other than in their normal localizations.
KILIÇ, HÜSEYİN KORAY +3 more
openaire +2 more sources
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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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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Therapeutics and Clinical Risk Management, 2019 Yun Feng, Jin-Ning Ye, Chuang-Qi Chen, Xin-Hua ZhangThe Center for Gastrointestinal Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510080, People’s Republic of ChinaAbstract: Gastric duplications are the least common ...
Feng Y, Ye JN, Chen CQ, Zhang XH
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Right Hemicolectomy in a Patient with Heterotaxy Syndrome
World Journal of Colorectal Surgery, 2019 In this communication, we present a first description of right hemicolectomy in a patient with heterotaxy syndrome (HS). A 78-year-old male was admitted to the outpatient clinic with complaints of dysphagia.
Maxime Dewulf +2 more
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Emergencies in neonatal management: jaundice and biliary atresia [PDF]
, 2016 Biliary atresia is a severe and progressive inflammatory process of unknown cause, which initially involves the extrahepatic bile ducts but which quickly proceeds towards the intrahepatic bile tree leading rapidly to biliary cirrhosis. Biliary atresia is
Clemente, Maria Grazia +1 more
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