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Diseases

Genetic and Rare Diseases Information Center (GARD)

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17q23.1q23.2 microdeletion syndrome


Other Names for this Disease

  • 17q23.1-q23.2 microdeletion syndrome
  • Chromosome 17q23.1-q23.2 deletion syndrome
  • Del(17)(q23.1q23.2)
  • Monosomy 17q23.1-q23.2
  • Monosomy 17q23.1q23.2
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Inheritance

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Is 17q23.2q23.2 microdeletion syndrome inherited?

Parental FISH testing in most of the reported cases confirmed a de novo origin, meaning that the deletion was new to the family.[1]
Last updated: 1/3/2013

References
  1. Morichon-Delvallez N. 17q23.1q23.2 microdeletion syndrome. Orphanet. 2011; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=261279. Accessed 1/2/2013.


Other Names for this Disease
  • 17q23.1-q23.2 microdeletion syndrome
  • Chromosome 17q23.1-q23.2 deletion syndrome
  • Del(17)(q23.1q23.2)
  • Monosomy 17q23.1-q23.2
  • Monosomy 17q23.1q23.2
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.