Chromosome 1p deletion
Other Names for this Disease
- Deletion 1p
- Monosomy 1p
- 1p deletion
- 1p monosomy
- Partial monosomy 1p
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chromosome abnormality that occurs when there is a missing copy of the genetic material located on the short arm (p) 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 1p 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 1p deletion is a
Last updated: 5/7/2015
- 1p Interstitial Deletions. Unique. 2009; http://www.rarechromo.org/information/Chromosome%20%201/1p%20interstitial%20deletions%20FTNW.pdf.
- Genetics Home Reference (GHR) contains information on Chromosome 1p 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 1p deletion.
1p interstitial deletions
1p36 deletion syndrome
- PubMed is a searchable database of medical literature and lists journal articles that discuss Chromosome 1p deletion. Click on the link to view a sample search on this topic.