Abstract

Cardiovascular abnormality is the most consistent finding and occur in almost 80 % of all Williams syndrome (WS). Although a number of cardiovascular defects are common to WS, the majority presents in some form of arterial stenosis whereas supravalvular aortic stenosis is the most common one. Here we describe a 12 year old boy with elfin facies, presenting with urinary incontinence and a systolic murmur in right upper parasternal region. Echocardiography showed presence of double chambered right ventricle (DCRV) along with supravalvular aortic stenosis (SVAS) and coronary artery aneurysms, left pulmonary artery stenosis and multiple bladder diverticula in CT abdomen. With the clinical suspicion the diagnosis of WS was made and confirmed by fluorescent in situ hybridisation (FISH) study showing deletion in 7q11.23. Though different forms of arterial stenosis at multiple sites have been demonstrated in WS, DCRV in Williams syndrome is not reported till date in medical literature.

Highlights

  • Williams syndrome constitutes of typical elfin facies, mental retardation, idiopathic hypercalcemia of infancy and supravalvular aortic stenosis (SVAS)

  • Williams syndrome has been shown to be due to a deletion involving the elastin gene on chromosome 7q11.23 (Pober 2010; Collins et al 2010a, b; Bernstein 2015)

  • In double chambered right ventricle (DCRV), a muscular band is present in the mid-right ventricular region, the band divides the chamber into two parts and creates obstruction between the inlet and

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Summary

Introduction

Background Williams syndrome constitutes of typical elfin facies, mental retardation, idiopathic hypercalcemia of infancy and supravalvular aortic stenosis (SVAS). In DCRV, a muscular band is present in the mid-right ventricular region, the band divides the chamber into two parts and creates obstruction between the inlet and *Correspondence: jayidoc@gmail.com 1 Department of Pediatrics, Calcutta National Medical College and Hospital, 24, Gorachand Road, Kolkata 700014, India Full list of author information is available at the end of the article outlet portions.

Results
Conclusion

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