Smith-Magenis Syndrome is a rare chromosomal disorder characterized by abnormalities of the head and facial (craniofacial) area, delays in the acquisition of skills requiring the coordination of mental and muscular activities (psychomotor retardation), mental retardation, speech delays, and/or behavioral abnormalities.

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GeneReviews: Smith-Magenis Syndrome
Summary, diagnosis, clinical description, differential diagnosis, management, genetic counseling and molecular genetics.
NORD: Smith Magenis Syndrome
Offers the synonyms, a general discussion and further resources.
PRISMS (Parents and Researchers Interested in Smith-Magenis Syndrome)
Details about the international support group organization and its mission as well as the condition. Includes an introduction, diagnosis, parent's corner, meet other people with SMS and educational considerations.
Taylor's Journey with Smith-Magenis Syndrome
Personal website that aims to help educate and provide support for other families coping with this condition.
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Last update:
March 21, 2015 at 16:39:09 UTC
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