Williams syndrome
From Health Encyclopedia
Contents |
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Used for
Beuren syndrome, elfin facies syndrome, Fanconi Schlesinger syndrome, idiopathic hypercalcemia supravalvular aortic stenosis, Williams Barratt syndrome, Williams Beuren syndrome
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Broader Terms
chromosome disorder, congenital disorder, syndrome
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Related Terms
aortic valve stenosis, hypercalcemia, mental retardation
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Scope Note
syndrome of elfinlike facies, mental retardation, growth deficiency, cardiovascular anomalies, and idiopathic infantile hypercalcemia.
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Facts (generated by robot; please edit if you find it inaccurate)
- " Another unusual aspect of Williams syndrome is that the onset of language is often delayed.
- Williams syndrome is not caused by anything the parents did or did not do either before or during pregnancy.
- Center for the Study of Autism, Salem, Oregon Williams Syndrome is a genetic disorder characterized by mild mental retardation.
- Williams syndrome is the deletion of one of the two #7 chromosomes and is missing the gene that makes the protein elastin (a protein which provides strength and elasticity to vessel walls) (3).
- DemographicsWilliams syndrome is estimated to occur in one of every 20,000 births.
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