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Directory of Williams Syndrome Resources

Home > Health > Conditions and Diseases > Neurological Disorders > Chromosomal > Williams Syndrome

Williams syndrome is a rare neurodevelopmental disorder caused by a deletion of about 26 genes from the long arm of chromosome 7. It is characterized by mental disability, heart defects and unusual facial features.

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Home > Health > Conditions and Diseases > Neurological Disorders > Chromosomal > Williams Syndrome

 


 

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