Williams syndrome (WS) is a rare genetic disorder caused by a micro-deletion of genes on chromosome 7, resulting in borderline to moderate levels of intellectual disability (Hillier et al., 2003; Mervis & John, 2010).
Williams syndrome (WS) is a relatively rare microdeletion disorder that occurs in as many as 1:7,500 individuals. WS arises due to the mispairing of low-copy DNA repetitive elements at meiosis.
Williams syndrome (WS) is a developmental condition caused by a deletion of 26–28 genes on one copy of chromosome 7q11.23. It is a relatively rare condition with an estimated prevalence of 1 in 7500 live births [ 1 ]. The WS phenotype is characterised by distinct medical, cognitive, and behavioural features.
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We describe the results of a functional and structural brain connectivity analysis comparing a homogeneous group of 10 young adults with Williams Syndrome (WS; 3 females, age 20. 7 ± 3.7 years, age range 17.4–28.7 years) to a group of 18 controls of similar age (3 females, age 23.9 ± 4.4 years, age range 16.8–30.2), with the aim to …
WS, Williams syndrome; FISH, fluorescence in situ hybridization. W illiams syndrome (WS, also Williams-INTRODUCTION Beuren syndrome), now recognized to be caused by a microdeletion of chromosome 7, is a multisystem disorder first identified as a dis-tinct clinical entity in 1961.1 It is present at birth and
Smith Williams died at his home in Twickenham the age of 77 in 1875, six months after retiring from business with George Smith, and is buried at Kensal Green Cemetery, London. The website of the Bronte Parsonage Museum and Bronte Society, Whats on at the Bronte Parsonage Museum Haworth West Yorkshire and What events are being run by the …
Williams syndrome (WS) is a rare genetic condition associated with high sociability, intellectual disability, and social cognitive challenges. Attention to others' eyes is crucial for social understanding. Orienting to, and from other's eyes was studied in WS (n = 37, mean age = 23, age range 9–53). The WS group was compared to a typically …
Introduction. Williams syndrome (WS) or Williams-Beuren syndrome (WBS) is a rare genetic multisystem disorder with an estimated prevalence of 1 in 7500 to 20000 live births [1,2].A deletion of approximately 25 genes causes this neuro-developmental condition in one copy of chromosome 7q11.23 []; which potentially causes dysmorphic …
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Williams Syndrome (WS) ... have rapidly switched to online-based activities. Although individuals with WS are characterized by high empathy and hypersociality, they simultaneously experience difficulties in social-communication and reciprocity skills, such as the ability to form and maintain friendships (19, 20). Thus, it is clear that ...
Williams syndrome (WS) is a rare neurodevelopmental disorder (~ 1/10,000 []) caused by a hemizygous deletion on chromosome band 7q11.23 and associated with a distinct socioaffective phenotype which includes an atypically strong drive for social engagement, an uninhibited propensity to approach and socially engage with strangers, …
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1 INTRODUCTION. Williams syndrome (WS), also known as Williams—Beuren syndrome, refers to a congenital developmental disorder, occurring in approximately 1:20 000 live births 1, 2 and involves both the connective and central nervous systems. 3 It is classified to the contiguous gene syndromes since the haploinsufficiency …
Abstract. We describe the results of a functional and structural brain connectivity analysis comparing a homogeneous group of 10 young adults with Williams Syndrome (WS; 3 females, age 20. 7 ± 3.7 years, age range 17.4–28.7 years) to a group of 18 controls of similar age (3 females, age 23.9 ± 4.4 years, age range 16.8–30.2), with …
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WS (also known as Williams-Beuren syndrome) is a rare neurodevelopmental disorder caused by a hemizygous microdeletion on chromosome 7 (7q11.23). The deletion is composed of approximately 26-28 genes and commonly includes one allele of the elastin gene, with an estimated prevalence of 1 in 7,500–10,000 live …
In this article, we discuss the case of Williams syndrome (WS), which is characterized by a set of missing genes on chromosome 7q11.23, and presents with a unique cognitive profile that includes severe spatial impairment along with strikingly fluent and well-structured language. An early inference from this profile was the idea that a …
About midway through the Phoenix Suns' season, Monty Williams passed screwdrivers out to his players. "We're all like, 'What is this?'" veteran forward Jae Crowder recently recalled ...
Williams syndrome (WS) is a relatively rare microdeletion disorder that occurs in as many as 1:7,500 individuals. It arises due to mispairing of low-copy DNA repetitive elements at meiosis. Deletion size is similar across most individuals with WS and leads to loss of one copy of 25–27 genes on chromosome 7q11.23. The resulting unique disorder ...
Introduction. Williams syndrome (WS), a neurodevelopmental disorder caused by a hemizygous deletion of up to 28 genes on chromosome 7q11.23 (Hillier et al., 2003), offers a unique opportunity to investigate interplays between gene, brain, and behavior.Cognitive hallmarks of WS include severe visuospatial deficits and relative …
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Social motivation in Williams syndrome. Atypical social motivation is a common facet of neuropsychiatric conditions including autism and depression and may act as a causal mechanism or treatment target 17, 18.In contrast, WS is seemingly a rare example of a condition which leads to enhanced rather than reduced social motivation 8.Studies of WS …
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Introduction. Williams syndrome (WS) (OMIM:194050) results from a microdeletion on chromosome 7q11.23 and is characterized by cardiovascular disease (CVD), distinctive face, intellectual disability, hypersocial behavior, short stature, and endocrine abnormalities. 1 The incidence is between 1:7500 and 1:25 000 live births. 2 …
Williams Syndrome, which is caused by deletions on chromosome 7q11, affects one in every 7,500 people. Children with Williams syndrome generally have striking social abilities while also navigating intellectual disability, predisposition for cardiovascular disease, and a variety of other medical conditions. Seeking to develop a comprehensive ...
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Williams syndrome (WS) is a rare genetic disorder caused by the deletion of approximately 28 genes on chromosome 7, and has a prevalence ranging from 1 in 7500 to 1 in 20,000 [1, 2].Along with its associated physical characteristics, such as dysmorphic facial features and heart defects, a unique hypersociable profile has been described [3, …
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Truman W. Williams was born on March 22, 1839, in Allegany County, New York to Asa and Louisa Keelar Williams. The Williams family consisted of at least one other child--a daughter named Rhoda Delana. The family later moved to Jefferson County, known as the "North Country" of New York state, to a small community of Burrville and later into …