Malrotation and volvulus associated with heterotaxy syndrome
Journal of Indian Association of Pediatric Surgeons, 2012 A 2-year-old boy with heterotaxy syndrome with associated polysplenia, ventricular septal defect, and malrotation of gut with volvulus is presented. There was delay in diagnosis due to the unusual plain abdominal radiography findings.
Santosh K Mahalik +2 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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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
doaj
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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Polysplenia syndrome associated to neonatal hepatitis
Jornal de Pediatria, 1998 OBJECTIVE: To report the unusual association between neonatal hepatitis and polysplenia syndrome.METHODS: Clinical, biochemical, histopathological, surgical and image analysis methods were used.RESULTS: The 36 days old patient presented hyperbilirubinemia with increase of direct reacting bilirubin and high alkaline phosphatase. The physical examination
J L, Santos +3 more
openaire +2 more sources
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
doaj
The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5 [PDF]
, 2016 G protein-coupled receptor kinase 5 (GRK5) is a regulator of cardiac performance and a potential therapeutic target in heart failure in the adult. Additionally, we have previously classified GRK5 as a determinant of left-right asymmetry and proper heart ...
Bauer, Ulrike M. M. +13 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
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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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Situs ambiguous and absence of the inferior vena cava: an extremely rare cause of femoral hemodialysis catheter dysfunction [PDF]
, 2015 Hemodialysis catheter dysfunction (CDys) has been defined by Kidney Disease utcomes Quality Initiative (K/DOQI) guidelines as “failure to maintain an extracorporeal blood flow sufficient to perform hemodialysis without significantly lengthening the ...
Castanha, Guida +3 more
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