Williams syndrome
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Williams syndrome
Williams syndrome, also called Williams-Beuren syndrome, is a genetic disorder that typically causes mild to moderate intellectual or learning disabilities, distinctive facial features, ...
Williams syndrome
Williams syndrome is a rare genetic disorder. Williams syndrome is characterised by distinctive physical features and behaviours including a distinctive facial appearance, ...
Williams Syndrome Causes, Symptoms and Treatment and Related Disorders ...
Williams Syndrome
National Organization for Rare Disorders, Inc.
Synonyms ...
Can Williams syndrome be inherited?
Most cases of Williams syndrome are not inherited, but occur as random events during the formation of reproductive cells (eggs or sperm) in a parent of an affected individual.
NINDS Williams Syndrome Information Page
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Williams syndrome is a rare condition caused by missing genes. Parents may not have any family history of the condition. However, a person with Williams syndrome has a 50% chance of passing the disorder on to each of his or her children.
Williams syndrome, Dementia, Lewy Body, Detoxication, Sorption, Didelphi, Disease Progressions, Dysostosis, Dystonia, Nocturnal Paroxysmal, Encephalopathy, Anoxic-Ischemic, Encephalopathy, Hypertensive, Endoderms, Estimate, Life Table, ...
Williams syndrome
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Williams Syndrome
Williams Syndrome Association - Support Group
Williams Syndrome Association - William's Syndrome - Support Group
Williams-Beuren Syndrome ...
Williams syndrome (Williams-Beuren syndrome) is a rare genetic disorder, occurring in fewer than 1 in every 20,000 live births.
Williams syndrome
Williams-Beuren syndrome see Williams syndrome
Wilson's disease see Liver disease
Winchester syndrome see Mucopolysaccharide diseases and Associated diseases
Wolf-Hirschhorn syndrome
Wolfram syndrome
Worster-Drought syndrome ...
Idiopathic infantile hypercalcemia (Williams syndrome—see Table 2: Chromosomal Anomalies: Examples of Contiguous Gene Syndromes) is an extremely rare sporadic disorder with dysmorphic facial features, cardiovascular abnormalities, ...
Genetic conditions such as Down syndrome, Turner syndrome, Williams syndrome, Russell-Silver syndrome, and Noonan syndrome
Bone or skeletal disorders such as rickets or achondroplasia ...
Children with Williams syndrome have trouble seeing spatial relationships between objects around them.
Those with Fragile X syndrome are often very sensitive to loud noises; they may overreact or have outbursts in reaction to such sounds.
Related Articles Amygdala response to faces parallels social behavior in Williams syndrome… more…
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The prevalence of absolute pitch is higher among those who are blind from birth as a result of optic nerve hypoplasia, and it has been claimed that it is higher among those with Williams Syndrome and those with an autism spectrum disorder.
 See also: Symptom, Mental retardation, Beuren syndrome, Stenosis, Hypothyroid
  
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