Chromosome 3q duplication
Other Names for this Disease
- Trisomy 3q
- Duplication 3q
- Chromosome 3, trisomy 3q
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chromosome abnormality that occurs when there is an extra copy of genetic material 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 duplication and which genes are involved. Features that often occur in people with chromosome 3q duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features. Chromosome 3q duplication can be de novo or inherited from a parent with a chromosomal rearrangement such as a balanced translocation. Treatment is based on the signs and symptoms present in each person.Chromosome 3q duplication is a
Last updated: 5/19/2015
- Duplications of 3q. Unique. 2008; http://www.rarechromo.org/information/Chromosome%20%203/3q%20duplications%20FTNW.pdf.
- Genetics Home Reference (GHR) contains information on Chromosome 3q duplication. This website is maintained by the National Library of Medicine.
- Unique is a source of information and support to families and individuals affected by rare chromosome disorders. Click on the link to view information about duplications of 3q.
- The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Chromosome 3q duplication. Click on the link to view a sample search on this topic.