About this campaign
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Lamb-Shaffer Syndrome is a genetic condition classified as a mutation, deletion or partial deletion of the SOX5 gene located in the 12th chromosome. The most common symptoms of Lamb-Shaffer Syndrome are, but not limited to, significant speech delay, hypotonia, gross motor delay, fine motor delay, global developmental delay, vision issues, mild facial abnormalities, a love of water, and a smile and laugh that could light up a room!
There are currently only approximately 500 people in the world diagnosed with this syndrome, but we KNOW there are more. Learn more at www.raisingarare.org
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