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Williams Syndrome Rebekah
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Published on Nov 18, 2015
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PRESENTATION OUTLINE
1.
WILLIAMS SYNDROME
A GENETIC DEVELOPMENTAL DISORDER
2.
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
3.
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.
4.
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
5.
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.
6.
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
7.
EVERYONE IS DIFFERENT, BUT WE'RE ALL HUMAN
THE END
Rebekah Perkins
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