Heterozygous deletion of the Williams–Beuren syndrome critical ...
Williams Syndrome Alexia Griffin. Williams Syndrome is a rare genetic disorder that can lead to...
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Transcript of Williams Syndrome Alexia Griffin. Williams Syndrome is a rare genetic disorder that can lead to...
Williams Syndrome is a rare genetic disorder that can lead to problems with development & can affect anyone. It is characterized by medical problems, including cardiovascular disease, development problems, and learning disabilities.
Symptoms
Sunken chest Unusual appearance of the face Flattened nasal bridge with small upturned
nose Long ridges in the skin that run from the
nose to the upper lip (philtrum) Prominent lips with an open mouth Skin that covers the inner corner of the eye
(epicanthal folds) Partially missing teeth, defective tooth
enamel, or small, widely spaced teeth
Delayed speech that may later turn into strong speaking ability and strong learning by hearing
Developmental delay Easily distracted, Attention Deficit Disorder (ADD) Feeding problems including colic, reflux, and vomiting Inward bend of the small finger Learning disorders Mild to moderate mental retardation Personality traits including being very friendly, trusting
strangers, fearing loud sounds or physical contact, and being interested in music
Short compared to the rest of the person's family
Personality traits including being very friendly, trusting strangers, fearing loud sounds or physical contact, and being interested in music.