Right juxtaposition of atrial appendages are rare and associated with congenital heart defects. We report 3 cases of right juxtaposition of atrial appendages (RJAA) diagnosed by transthoracic echocardiography. The sub-xiphoid sagittal view, parasternal short axis and apical four chambered views demonstrated RJAA. All 3 cases with RJAA were associated with congenital heart disease. Diagnosis was confirmed by CT angiogram and intra-operative findings in two children who underwent surgical correction. Right juxtaposition of atrial appendages is a rare association with congenital heart defects. Transthoracic echocardiographic assessment may give clues to the diagnosis
The results are reported of a study of 83 necropsied hearts with atresia of the right atrioventricul...
A 9-year-old female was referred to our institution with a history of palpitations at rest. She had...
A prenatal diagnosis of right atrial isomerism is often inferred through the recognition of a conste...
Juxtaposition of the atrial appendages is a rare congenital cardiac malformation, with the appendage...
Juxtaposition of the atrial appendages is an apparently rare congenital cardiac anomaly in which the...
A 13-month-old boy with a diagnosis of atrial septal defect and pulmonary valve stenosis was admitte...
Left juxtaposition of the atrial appendages is usually associated with cyanotic congenital heart dis...
The frequent association of complex congenital heart defects and left juxtaposition of atrial append...
Juxtaposition of the atrial appendages is a rare congenital cardiac malformation, with the appendage...
Left juxtaposition of the atrial appendages (LJAA) is a rare anomaly in which the two atrial appenda...
Juxtaposition of atrial appendages is a rare cardiac congenital anomaly, usually associated with oth...
AbstractIn a prospective investigation, direct visualization of both atrial appendages was attempted...
The case of an infant with double outlet right ventricle with anatomically corrected malposition of ...
AbstractCongenital aneurysm of the right atrial appendage is a rare cardiac anomaly with only a few ...
Left atrial appendage aneurysm (LAAA) is a rare cardiac anomaly, the association with right ventricu...
The results are reported of a study of 83 necropsied hearts with atresia of the right atrioventricul...
A 9-year-old female was referred to our institution with a history of palpitations at rest. She had...
A prenatal diagnosis of right atrial isomerism is often inferred through the recognition of a conste...
Juxtaposition of the atrial appendages is a rare congenital cardiac malformation, with the appendage...
Juxtaposition of the atrial appendages is an apparently rare congenital cardiac anomaly in which the...
A 13-month-old boy with a diagnosis of atrial septal defect and pulmonary valve stenosis was admitte...
Left juxtaposition of the atrial appendages is usually associated with cyanotic congenital heart dis...
The frequent association of complex congenital heart defects and left juxtaposition of atrial append...
Juxtaposition of the atrial appendages is a rare congenital cardiac malformation, with the appendage...
Left juxtaposition of the atrial appendages (LJAA) is a rare anomaly in which the two atrial appenda...
Juxtaposition of atrial appendages is a rare cardiac congenital anomaly, usually associated with oth...
AbstractIn a prospective investigation, direct visualization of both atrial appendages was attempted...
The case of an infant with double outlet right ventricle with anatomically corrected malposition of ...
AbstractCongenital aneurysm of the right atrial appendage is a rare cardiac anomaly with only a few ...
Left atrial appendage aneurysm (LAAA) is a rare cardiac anomaly, the association with right ventricu...
The results are reported of a study of 83 necropsied hearts with atresia of the right atrioventricul...
A 9-year-old female was referred to our institution with a history of palpitations at rest. She had...
A prenatal diagnosis of right atrial isomerism is often inferred through the recognition of a conste...