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- W4310251743 abstract "Abstract Characterized by congenital heart defects (CHD) and elfin-like facies, Williams-Beuren syndrome (WS) is a multisystemic disorder that occurs approximately in 1 in 10 000 newborns [1]. WS is caused by a contiguous gene microdeletion of the Williams Beuren syndrome critical region (WBSCR) on chromosome 7q11.23, resulting in an abnormal elastin gene (ELN). There is a wide range of CHD in patients with WS, with supravalvular aortic stenosis (SAS) being the most common, and atypically the atrial septal defect (ASD) [2]. Few reports and reviews have linked the appearance of ASD to WS. Thus, data on the management of ASD secondary to WS is not well-documented. The following case report consists of the diagnosis and management of an ASD in a pediatric patient with WS." @default.
- W4310251743 created "2022-11-30" @default.
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- W4310251743 date "2022-11-01" @default.
- W4310251743 modified "2023-10-14" @default.
- W4310251743 title "Atrial septal defect in a pediatric patient with Williams Syndrome: a rare presentation" @default.
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- W4310251743 doi "https://doi.org/10.1093/jscr/rjac527" @default.
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