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Williams syndrome includes upturn nose, long upper lip, wide mouth, full lips, small chin and puffiness around the eyes.
The chromosome it affects is chromosome 7 . Missing material on the chromosome
Williams syndrome affects boys and girls equally. It  happens at a young age like infants.
Some affects of William syndrome are learning disorder mild  mental retardationvery friendly, fearing loud sounds.
The parts of the body effects is all the parts of the body face, brain etc.
There is no cure for Williams syndrome but many affected children and adults lead full and active lives.
This is what Williams syndrome related toBeuren Syndrome Early Hypercalcemia Syndrome with Elfin Facies Elfin Facies with Hypercalcemia Hypercalcemia-Supravalar Aortic Stenosis WBS Williams-Beuren Syndrome WMS
In the early 1990s, researchers located and identified the genetic mutation responsible for the disorder: the deletion of a small section of chromosome 7 that contains approximately 25 genes
Three things I didn’t tell you isit is a very rare diseasein 1/10,000 births it occurs
works cited  http://www.williams –syndrome.org/forparents/whatiswilliams.html#1 http:b//learn.genetics.utah.edu/content/disorders/whataregd/williams/ http://ghr.nlm.nih.gov/condition=williamssyndrome http://www.ninds.nih.gov/disorders /Williams/Williams.htm http://www.ninds.nihgov/disorders/williams/williams.htm

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Williams Syndrome susquenita

  • 1.
  • 2. Williams syndrome includes upturn nose, long upper lip, wide mouth, full lips, small chin and puffiness around the eyes.
  • 3. The chromosome it affects is chromosome 7 . Missing material on the chromosome
  • 4. Williams syndrome affects boys and girls equally. It happens at a young age like infants.
  • 5. Some affects of William syndrome are learning disorder mild mental retardationvery friendly, fearing loud sounds.
  • 6. The parts of the body effects is all the parts of the body face, brain etc.
  • 7. There is no cure for Williams syndrome but many affected children and adults lead full and active lives.
  • 8. This is what Williams syndrome related toBeuren Syndrome Early Hypercalcemia Syndrome with Elfin Facies Elfin Facies with Hypercalcemia Hypercalcemia-Supravalar Aortic Stenosis WBS Williams-Beuren Syndrome WMS
  • 9. In the early 1990s, researchers located and identified the genetic mutation responsible for the disorder: the deletion of a small section of chromosome 7 that contains approximately 25 genes
  • 10. Three things I didn’t tell you isit is a very rare diseasein 1/10,000 births it occurs
  • 11. works cited http://www.williams –syndrome.org/forparents/whatiswilliams.html#1 http:b//learn.genetics.utah.edu/content/disorders/whataregd/williams/ http://ghr.nlm.nih.gov/condition=williamssyndrome http://www.ninds.nih.gov/disorders /Williams/Williams.htm http://www.ninds.nihgov/disorders/williams/williams.htm