A rare cause of syncope: Cor triatriatum

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Cor triatriatum sinister: a rare underlying cause of pulmonary hemosiderosis

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Adult cor triatriatum sinistrum: a rare cause of ischaemic stroke

A 55-year-old male was referred to the cardiologist because of the occurrence of two ischaemic strokes within five months’ time in the absence of documented atrial fibrillation. At echocardiography, a membrane was visualised in the left atrium (cor triatriatum) (Fig. 1a). Since no other abnormalities were detected, the cor triatriatum was held responsible for the cardioembolic stroke. Surgical ...

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Cor triatriatum in a young woman with syncope.

1 of 3 DESCRIPTION A 28-year-old woman presented with recurrent syncope, usually precipitated by anxiety. On examination, she had a low blood pressure of 112/72 mm Hg with normal heart sounds and showed no features suggestive of genetic abnormalities. ECG, Holter and treadmill stress tests were normal. Transthoracic ( fi gure 1 ) and transoesophageal ( fi gure 2 ) echocardiography demonstrated ...

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Cor triatriatum sinister.

C triatriatum is a very rare congenital cardiac anomaly with no known associated genetic abnormalities. Cor triatriatum is generally an isolated anomaly but may be associated with anomalous pulmonary venous return in approximately 10% of patients, patent ductus arteriosus, left superior vena cava, ventricular septal defects, Shone syndrome, tricuspid atresia, Ebstein malformation, atrioventricu...

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Cor Triatriatum Sinistrum Presenting as Cyanotic Congenital Heart Disease A Rare Case Report

  Cor triatriatum is an acyanotic congenital heart disease. We present a rare case of cor triatriatum sinistrum in a 6-month-old female infant who was presented with cyanosis and failure to thrive. The 2D transthoracic echocardiography and the Doppler color flow imaging showed a proximal venous chamber communicating to the distal left atrium  through restrictive opening to the low-pressure, dis...

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ژورنال

عنوان ژورنال: Turkish Journal of Emergency Medicine

سال: 2013

ISSN: 1304-7361

DOI: 10.5505/1304.7361.2013.16046