Chromosome 1q deletion
Other Names for this Disease
- Deletion 1q
- Monosomy 1q
- 1q deletion
- 1q monosomy
- Partial monosomy 1q
chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 1. 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 1q deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. 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.Chromosome 1q deletion is a
Last updated: 5/7/2015
- 1q4 deletions: from 1q42 and beyond. Unique. 2013; http://www.rarechromo.org/information/Chromosome%20%201/1q4%20deletions%20FTNW.pdf.
- Genetics Home Reference (GHR) contains information on Chromosome 1q deletion. This website is maintained by the National Library of Medicine.
- Unique is a source of information and support for families and individuals affected by rare chromosome disorders. Click on the link to view information about Chromosome 1q deletion.
1q4 deletions: from 1q42 and beyond
- PubMed is a searchable database of medical literature and lists journal articles that discuss Chromosome 1q deletion. Click on the link to view a sample search on this topic.