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Smith-Magenis syndrome

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Smith-Magenis syndrome (SMS) is a complex genetic disorder characterized by variable intellectual deficit, sleep disturbance, craniofacial and skeletal anomalies, psychiatric disorders, and speech and motor delay.

Synonyms

  • 17p11.2 microdeletion syndrome
  • SMITH-Magenis syndrome
  • SMS
  • Smith Magenis Syndrome
  • Smith-Magenis chromosome region
  • Smith-Magenis syndrome
  • Smith-Magenis syndrome chromosome region
  • Smith-Magenis syndrome, Isolated cases
  • chromosome 17P11.2 deletion syndrome
  • chromosome 17p11.2 deletion syndrome17p11.2 microdeletion syndrome
  • SMITH-Magenis syndrome
  • SMS
  • Smith Magenis Syndrome
  • Smith-Magenis chromosome region
  • Smith-Magenis syndrome
  • Smith-Magenis syndrome chromosome region
  • Smith-Magenis syndrome, Isolated cases
  • chromosome 17P11.2 deletion syndrome
  • chromosome 17p11.2 deletion syndrome
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