syndrome

(redirected from Budd-Chiari syndrome)
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References in periodicals archive ?
The treatment options for Budd-Chiari syndrome are well established and include medical management, endovascular procedures, and surgical interventions.
First, understanding the pathophysiology of Budd-Chiari syndrome is crucial to the success of interventional treatments, especially in DIPS.
Role of JAK 2 mutation detection in Budd-Chiari syndrome (BCS) and portal vein thrombosis (PVT) associated to MPD.
Successful stenting for Budd-Chiari syndrome after pediatric liver transplantation: a case series and review of the literature.
Bleeding in patients with Budd-Chiari Syndrome. Journal of Hematology.
Paroxysmal nocturnal haemoglobinuria revealed by hepatic vein thrombosis (Budd-Chiari syndrome) during infliximab therapy.
Budd-Chiari syndrome associated with antiphospholipid antibodies in a child: report of a case and review of the literature.
Pulmonary artery aneurysm accounted for 7%, superior vena cava syndrome 5%, and Budd-Chiari syndrome secondary to hepatic vein stenosis 3.8%, with lesser numbers of aortic and carotid artery aneurysms and inferior vena cava involvement.
Q MY daughter has Budd-Chiari syndrome. I know it concerns the liver but can you give us more details?
The imaging and pathologic findings are consistent with Budd-Chiari syndrome. There was no evidence of either benign or malignant intrahepatic neoplasm.
Hyperhomocysteinaemia and factor V Leiden mutation are associated with Budd-Chiari syndrome. Eur J Gastroenterol Hepatol 2006;18:917-20.
A British pathologist concluded the 56-year-old died from Budd-Chiari syndrome, a rare liver disorder that results from blood clotting in the veins flowing out of it.