Due to high mortality associated with aortic dissection, anesthetic management of patients with Marfan syndrome with severe aortic root dilation is a challenging situation. We describe the anesthetic management of a patient with Marfan syndrome with severe aortic root dilation, who required major surgery like cholecystectomy with partial liver resection under general anesthesia. A 47-year-old female presented to pre-anesthetic clinic for cholecystectomy with partial hepatic resection for gall bladder carcinoma. Clinical features, transthoracic echocardiography and computed tomography of thorax supported a diagnosis of Marfan syndrome with severely dilated aortic root. Aortic dissection in patients with Marfan syndrome and severely dilated a...
Marfan’s syndrome is an autosomal dominant disorder of connective tissue affecting approximately1 in...
Objective: To describe perioperative management for type A aortic dissection in a postpartum woman w...
WOS: 000223919800004PubMed: 15529906A 7-year-old girl was admitted because of dyspnea on exertion an...
AbstractBackgroundMarfan's Syndrome (MFS) is a disorder of connective tissue, mainly involving the c...
Abstract Background: Marfan's Syndrome (MFS) is a disorder of connective tissue, mainly involving t...
Cardiovascular disease is the main cause of morbidity and mortality in patients with Marfan syndrome...
We report a case of a female patient with Marfan syndrome who suffered a type A acute aortic dissect...
This report describes the hybrid endovascular treatment of an aortic root dilatation and a thoracoab...
Marfan syndrome is the most common inherited disorder of connective tissue affecting multiple organ ...
Acute dissection and rupture of aortic aneurysms comprise for 1-2% of all deaths in industrialized c...
This report describes the hybrid endovascular treatment of an aortic root dilatation and a thoracoab...
Marfan syndrome is a heritable connective tissue disorder.The cardiovascular effects are life-threat...
In order to examine the incidence of aortic (Ao) complications in Marfan's syndrome, and the relatio...
Introduction. Marfan syndrome (MFS) is a rare connective tissue disorder attributed to a defect in t...
Marfan syndrome is an autosomal dominant inherited disorder of connective tissue, with various compl...
Marfan’s syndrome is an autosomal dominant disorder of connective tissue affecting approximately1 in...
Objective: To describe perioperative management for type A aortic dissection in a postpartum woman w...
WOS: 000223919800004PubMed: 15529906A 7-year-old girl was admitted because of dyspnea on exertion an...
AbstractBackgroundMarfan's Syndrome (MFS) is a disorder of connective tissue, mainly involving the c...
Abstract Background: Marfan's Syndrome (MFS) is a disorder of connective tissue, mainly involving t...
Cardiovascular disease is the main cause of morbidity and mortality in patients with Marfan syndrome...
We report a case of a female patient with Marfan syndrome who suffered a type A acute aortic dissect...
This report describes the hybrid endovascular treatment of an aortic root dilatation and a thoracoab...
Marfan syndrome is the most common inherited disorder of connective tissue affecting multiple organ ...
Acute dissection and rupture of aortic aneurysms comprise for 1-2% of all deaths in industrialized c...
This report describes the hybrid endovascular treatment of an aortic root dilatation and a thoracoab...
Marfan syndrome is a heritable connective tissue disorder.The cardiovascular effects are life-threat...
In order to examine the incidence of aortic (Ao) complications in Marfan's syndrome, and the relatio...
Introduction. Marfan syndrome (MFS) is a rare connective tissue disorder attributed to a defect in t...
Marfan syndrome is an autosomal dominant inherited disorder of connective tissue, with various compl...
Marfan’s syndrome is an autosomal dominant disorder of connective tissue affecting approximately1 in...
Objective: To describe perioperative management for type A aortic dissection in a postpartum woman w...
WOS: 000223919800004PubMed: 15529906A 7-year-old girl was admitted because of dyspnea on exertion an...