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Genetic and Rare Diseases Information Center (GARD)

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Chromosome 3q deletion


Other Names for this Disease
  • 3q deletion
  • 3q monosomy
  • Deletion 3q
  • Monosomy 3q
  • Partial monosomy 3q
Related Diseases
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Overview

Chromosome 3q deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 3. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with chromosome 3q deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features.[1] Most cases are not inherited, but people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person.
Last updated: 6/15/2015

References

  1. Almenrader N, Passariello M, Coccetti B, Pietropaoli P. Anesthesia for a child with deletion 3q syndrome. Paediatr Anaesth. August 2008; 18(8):789-790.
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Basic Information

In Depth Information

  • PubMed is a searchable database of medical literature and lists journal articles that discuss Chromosome 3q deletion. Click on the link to view a sample search on this topic.
Other Names for this Disease
  • 3q deletion
  • 3q monosomy
  • Deletion 3q
  • Monosomy 3q
  • Partial monosomy 3q
Related Diseases
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.