Many patients with congenital cardiac disease are at risk for progressive aortic dilation. The mechanisms underlying aortic dilation in this patient cohort are described, and the similarities to the pathophysiologic alterations seen in Marfan syndrome are highlighted. Indications for treatment are discussed
The dramatic reductions in DNA sequencing costs allow us to delve deeper into the genomic alteration...
BackgroundIn patients with Marfan syndrome, progressive aortic dilation implicates a still-unpredict...
Objectives Patients with Marfan syndrome (MFS) are prone to develop aortic aneurysms due to fragment...
AbstractObjectives. The present study examines the incidence of aortic complications (dissection, ma...
In patients born with congenital heart disease, dilatation of the aorta is a frequent feature at pre...
ObjectivesThere is increasing attention to prophylactic replacement of the moderately dilated ascend...
AbstractLonger survival after corrective surgery for congenital heart diseases has rendered late com...
Acute dissection and rupture of aortic aneurysms comprise for 1-2% of all deaths in industrialized c...
Thoracic aortic dilation (AD) has commonly been described in conotruncal defects (CTDs), such as tet...
Objective: Dilatation of the aortic root is a well-known cardiovascular manifestation in children an...
Aims The main aim of this study was to describe the age at which pathological aortic root dilation o...
Marfan syndrome is the most common inherited disorder of connective tissue affecting multiple organ ...
Thoracic aortic aneurysms can be triggered by genetic disorders such as Marfan syndrome (MFS) and re...
ObjectiveAortic complications determine the life expectancy of most patients with Marfan syndrome. T...
Aims The main aim of this study was to describe the age at which pathological aortic root dilation o...
The dramatic reductions in DNA sequencing costs allow us to delve deeper into the genomic alteration...
BackgroundIn patients with Marfan syndrome, progressive aortic dilation implicates a still-unpredict...
Objectives Patients with Marfan syndrome (MFS) are prone to develop aortic aneurysms due to fragment...
AbstractObjectives. The present study examines the incidence of aortic complications (dissection, ma...
In patients born with congenital heart disease, dilatation of the aorta is a frequent feature at pre...
ObjectivesThere is increasing attention to prophylactic replacement of the moderately dilated ascend...
AbstractLonger survival after corrective surgery for congenital heart diseases has rendered late com...
Acute dissection and rupture of aortic aneurysms comprise for 1-2% of all deaths in industrialized c...
Thoracic aortic dilation (AD) has commonly been described in conotruncal defects (CTDs), such as tet...
Objective: Dilatation of the aortic root is a well-known cardiovascular manifestation in children an...
Aims The main aim of this study was to describe the age at which pathological aortic root dilation o...
Marfan syndrome is the most common inherited disorder of connective tissue affecting multiple organ ...
Thoracic aortic aneurysms can be triggered by genetic disorders such as Marfan syndrome (MFS) and re...
ObjectiveAortic complications determine the life expectancy of most patients with Marfan syndrome. T...
Aims The main aim of this study was to describe the age at which pathological aortic root dilation o...
The dramatic reductions in DNA sequencing costs allow us to delve deeper into the genomic alteration...
BackgroundIn patients with Marfan syndrome, progressive aortic dilation implicates a still-unpredict...
Objectives Patients with Marfan syndrome (MFS) are prone to develop aortic aneurysms due to fragment...