Wednesday, April 8, 2009
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Resources and updates from the Web on Williams Syndrome
Williams Syndrome
Identified more than 40 years ago, Williams syndrome occurs in an estimated one in 20,000 births worldwide. It arises from a faulty recombination event during the development of sperm or egg cells. As a result, almost invariably the same set of about 20 genes surrounding the gene for elastin is deleted from one copy of chromosome seven, catapulting the carrier of the deletion into a world where people make much more sense than objects do. Despite a myriad of health problems and a generally low IQ, people with Williams syndrome are loquacious, sociable, and very empathetic.
Why This Blog?
I am a Dad to a great little WS person and love doing all I can to understand his world and love him better. Since information on WS is fairly rare, I thought I would share whatever I found of interest. Plus, if you know my kid, here is a great way for you to understand him better!
Search by Category
- Books on Williams Syndrome (5)
- Diagnosis (3)
- Fundraising (14)
- Human Interest (74)
- Medical Care (38)
- Music (13)
- Occupation (3)
- Parental Experience (10)
- Research (6)
- Resources (17)
- Understanding WS (54)
- Video (18)
Posts
Archive
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2009
(78)
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April
(12)
- Williams Syndrome Researcher Named to American Aca...
- Running for Sophie
- Williams Syndrome: UD Research Pinpoints Language ...
- New Research on How Williams Syndrome Effects Qual...
- Daily Dispatch Online
- New Book on Cognitive Development in Williams Synd...
- Williams Syndrome on Facebook
- Retinotopically defined primary visual cortex in W...
- Language Use in Williams Syndrome
- Black River student travels to Middle East - Holla...
- Strange Science?
- New Help for Williams Syndrome Diagnosis?
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April
(12)
My personal blog...
Did We Miss Something?
Got something you think should be posted at WSWW? Send us an email with a link at "the[dot]kerux[at]gmail[dot]com"
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