Williams–Beuren syndrome is a multisystem genetic disorder caused by hemizygous deletion on chromosome 7q11.23, encompassing about 28 genes including the elastin gene, ELN. Cardiovascular abnormalities are frequent and are related to elastin insufficiency. These abnormalities include supravalvular aortic stenosis (SVAS) in 70% of case, pulmonic valve stenosis, and renal artery stenosis. Definitive therapy for supravalvar aortic stenosis consists of surgical correction of the arteriopathies. Outcomes after surgical correction of SVAS depend on the extent of the arteriopathy and the presence of other associated lesions. We present a case of a 4-year-old boy, with Williams - Beuren syndrome with an SVAS. The patient was assessed with computeri...
Williams syndrome (WS) is a developmental disorder characterized by vascular abnormalities such as t...
Williams-Beuren Syndrome (WB-S) occurs in ap-proximately 1/7500 live births. It is characterized by ...
BACKGROUND AND PURPOSE: Williams syndrome, a rare genetic disorder with a striking neurobehavioral p...
Supravalvular aortic stenosis is associated with the Williams–Beuren syndrome, but it also occurs in...
OBJECTIVE: To evaluate the cardiovascular findings and clinical follow-up of patients with Williams-...
Copyright © 2012 Hassan Zamani et al. This is an open access article distributed under the Creative ...
We report the case of a 7-year-old male child diagnosed with Williams-Beuren syndrome and arterial h...
4 months male child presented with failure to thrive. On general examination child had normal O2 sat...
The 7q11.23 microduplication syndrome, caused by the reciprocal duplication of the Williams-Beuren s...
Abstract: Williams-Beuren syndrome (WBS) is a rare, microdeletion syndrome characterized by facial d...
International audienceObjective. To estimate the frequency and investigate the clinical features of ...
Abstract4 months male child presented with failure to thrive. On general examination child had norma...
Supravalvular aortic stenosis is usually diagnosed and corrected in childhood. An adult patient with...
Supravalvular aortic stenosis (SVAS) is a localized or diffuse congenital narrowing of the ascending...
Aims: To define the cardiovascular anomalies and the long- term outcomes in an Asian cohort with Wil...
Williams syndrome (WS) is a developmental disorder characterized by vascular abnormalities such as t...
Williams-Beuren Syndrome (WB-S) occurs in ap-proximately 1/7500 live births. It is characterized by ...
BACKGROUND AND PURPOSE: Williams syndrome, a rare genetic disorder with a striking neurobehavioral p...
Supravalvular aortic stenosis is associated with the Williams–Beuren syndrome, but it also occurs in...
OBJECTIVE: To evaluate the cardiovascular findings and clinical follow-up of patients with Williams-...
Copyright © 2012 Hassan Zamani et al. This is an open access article distributed under the Creative ...
We report the case of a 7-year-old male child diagnosed with Williams-Beuren syndrome and arterial h...
4 months male child presented with failure to thrive. On general examination child had normal O2 sat...
The 7q11.23 microduplication syndrome, caused by the reciprocal duplication of the Williams-Beuren s...
Abstract: Williams-Beuren syndrome (WBS) is a rare, microdeletion syndrome characterized by facial d...
International audienceObjective. To estimate the frequency and investigate the clinical features of ...
Abstract4 months male child presented with failure to thrive. On general examination child had norma...
Supravalvular aortic stenosis is usually diagnosed and corrected in childhood. An adult patient with...
Supravalvular aortic stenosis (SVAS) is a localized or diffuse congenital narrowing of the ascending...
Aims: To define the cardiovascular anomalies and the long- term outcomes in an Asian cohort with Wil...
Williams syndrome (WS) is a developmental disorder characterized by vascular abnormalities such as t...
Williams-Beuren Syndrome (WB-S) occurs in ap-proximately 1/7500 live births. It is characterized by ...
BACKGROUND AND PURPOSE: Williams syndrome, a rare genetic disorder with a striking neurobehavioral p...