Your browser does not support javascript:   Search for gard hereSearch for news-and-events here.

Diseases

Genetic and Rare Diseases Information Center (GARD)

Print friendly version

Smith-Magenis syndrome


Other Names for this Disease

  • Chromosome 17p11.2 deletion syndrome
  • SMS
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Inheritance

Newline Maker

Is Smith-Magenis syndrome inherited?

Smith-Magenis syndrome is not typically inherited. The condition usually results from a genetic change that occurs during the formation of reproductive cells (eggs or sperm) or in early fetal development. Most often, people with Smith-Magenis syndrome have no history of the condition in their family.[1][2] In a very small number of cases, parental mosaicism has been reported. Complex familial chromosomal rearrangements leading to deletion of chromosome 17p11.2 and Smith-Magenis syndrome have also been reported. Again, these are very rare. As a result, chromosome analysis of the parents is suggested for all newly diagnosed individuals. This information can help to identify specific risks to other family members. For instance, if a parent of an individual with Smith-Magenis syndrome has a balanced chromosome rearrangement, at-risk family members (siblings, etc.) can be tested by chromosome analysis and FISH.[2]
Last updated: 2/15/2012

References
  1. Smith-Magenis syndrome. Genetics Home Reference (GHR). 2007; http://ghr.nlm.nih.gov/condition=smithmagenissyndrome. Accessed 2/15/2012.
  2. Smith ACM et al.. Smith-Magenis Syndrome - Genetic Counseling. GeneReviews. January 7, 2010; http://www.ncbi.nlm.nih.gov/books/NBK1310/#sms.Genetic_Counseling. Accessed 2/15/2012.


Other Names for this Disease
  • Chromosome 17p11.2 deletion syndrome
  • SMS
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.