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Williams Syndrome Rebekah

Published on Nov 18, 2015

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PRESENTATION OUTLINE

WILLIAMS SYNDROME

A GENETIC DEVELOPMENTAL DISORDER

WHAT IS IT?

  • WS is a condition that affects many parts of your body
  • Your heart, arteries, kidneys, muscles, and your senses all are affected
  • When you have WS, you are missing a chunk of genetic material
  • The missing pieces are from Chromosome 7
  • You can have over 25 different missing genes with WS

HOW IS WS PASSED?

  • Williams Syndrome is usually passed down randomly
  • Most families have no history of the syndrome
  • There is a fifty fifty chance of passing it onto your child if inflicted
  • Again, the syndrome affects Chromosome 7
  • A section of genetic material is delected, and removes certain genes.

WHO DOES IT AFFECT?

  • Williams Syndrome affects everyone
  • Men and women have equal chances of having WS
  • Affects between every one and 7500-20000 people
  • 75% of people with WS live in a group home/with caregivers
  • Many people with this disease do not live long due to complications

SYMPTOMS OF WS

  • Prominent facial features
  • Heart and blood vessel problems
  • Abnormalities in teeth, kidneys and muscles
  • Sensitive hearing and sight
  • Overly friendly, a lacy or starburst pattern on eyes.

TREATMENT OPTIONS

  • No official treatment currently exists
  • Corrective surgery for veins/blood vessels
  • Forms of therapy like:
  • Physical, development, speech and music therapy
  • Coordinated treatment with a geneticist

EVERYONE IS DIFFERENT, BUT WE'RE ALL HUMAN

THE END