The Williams-Beuren syndrome, a rare congenital anomaly involving the vascular system, connective tissue, and central nervous system, was initially described by Williams et al in 1961, and then by ...

A rare genetic disorder, Williams Syndrome, affects around 1 in 7,500 to 10,000 people worldwide. It is caused by the deletion of a small segment of chromosome 7, which contains 25–27 genes.

Williams syndrome, which affects 30,000 people in the U.S., ... about 26 to 28 missing genes on chromosome 7. There are some serious symptoms, like intellectual disability, ...

Williams Syndrome (WS), or Williams-Beuren Syndrome, is a rare sporadic genetic disorder that appears in approximately 1 of every 10,000-20,000 people worldwide [1].It is the result of missing genetic ...

Abstract. Introduction Williams syndrome (WS) is a genetic disorder caused by a microdeletion in chromosome 7, affecting ~ 28 genes.Studies have demonstrated conductive losses seemingly related to the ...

Background. Williams–Beuren syndrome (WBS) was first described in 1961.1 It is a rare genetic syndrome with a prevalence of approximately one in 10 000–20 000 births in the USA or a prevalence of ...

Williams syndrome is a rare genetic disorder that is caused by the deletion of genetic material on chromosome 7. Typical characteristics include distinctive facial features, mild intellectual ...

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For Williams syndrome, caused by the spontaneous deletion of genetic material from chromosome 7, like with Edwards’ syndrome, managing symptoms is key. Cardiovascular issues are handled through ...