Williams syndrome is a well-recognised congenital disorder characterised by cardiovascular, connective tissue, and central nervous system abnormalities. Coronary artery abnormalities are seen in patients with supravalvar aortic stenosis, but end-stage ischaemic heart disease is rare. We report a case of end-stage ischaemic heart disease due to severe coronary arterial stenosis, highlighting how cardiovascular MRI contributed to the management
AbstractObjectives. We used intraluminal ultrasound imaging to provide additional information about ...
AbstractSupravalvular aortic stenosis is the rarest form of congenital left ventricular outflow trac...
Supravalvular aortic stenosis is associated with the Williams–Beuren syndrome, but it also occurs in...
Background: Sudden death risk in Williams syndrome (WS) patients has been shown to be 25–100 t...
Williams–Beuren syndrome is a multisystem genetic disorder caused by hemizygous deletion on chromoso...
Abstract: Williams-Beuren syndrome (WBS) is a rare, microdeletion syndrome characterized by facial d...
Williams syndrome (WS) is a developmental disorder characterized by vascular abnormalities such as t...
4 months male child presented with failure to thrive. On general examination child had normal O2 sat...
Copyright © 2012 Hassan Zamani et al. This is an open access article distributed under the Creative ...
OBJECTIVE: To evaluate the cardiovascular findings and clinical follow-up of patients with Williams-...
Aims: To define the cardiovascular anomalies and the long- term outcomes in an Asian cohort with Wil...
Abstract4 months male child presented with failure to thrive. On general examination child had norma...
A 15-year-old girl was admitted because of an acute onset of facial palsy and right hemiparesis. The...
BACKGROUND AND PURPOSE: Williams syndrome, a rare genetic disorder with a striking neurobehavioral p...
Supravalvular aortic stenosis is usually diagnosed and corrected in childhood. An adult patient with...
AbstractObjectives. We used intraluminal ultrasound imaging to provide additional information about ...
AbstractSupravalvular aortic stenosis is the rarest form of congenital left ventricular outflow trac...
Supravalvular aortic stenosis is associated with the Williams–Beuren syndrome, but it also occurs in...
Background: Sudden death risk in Williams syndrome (WS) patients has been shown to be 25–100 t...
Williams–Beuren syndrome is a multisystem genetic disorder caused by hemizygous deletion on chromoso...
Abstract: Williams-Beuren syndrome (WBS) is a rare, microdeletion syndrome characterized by facial d...
Williams syndrome (WS) is a developmental disorder characterized by vascular abnormalities such as t...
4 months male child presented with failure to thrive. On general examination child had normal O2 sat...
Copyright © 2012 Hassan Zamani et al. This is an open access article distributed under the Creative ...
OBJECTIVE: To evaluate the cardiovascular findings and clinical follow-up of patients with Williams-...
Aims: To define the cardiovascular anomalies and the long- term outcomes in an Asian cohort with Wil...
Abstract4 months male child presented with failure to thrive. On general examination child had norma...
A 15-year-old girl was admitted because of an acute onset of facial palsy and right hemiparesis. The...
BACKGROUND AND PURPOSE: Williams syndrome, a rare genetic disorder with a striking neurobehavioral p...
Supravalvular aortic stenosis is usually diagnosed and corrected in childhood. An adult patient with...
AbstractObjectives. We used intraluminal ultrasound imaging to provide additional information about ...
AbstractSupravalvular aortic stenosis is the rarest form of congenital left ventricular outflow trac...
Supravalvular aortic stenosis is associated with the Williams–Beuren syndrome, but it also occurs in...