Chromosome 2q deletion: Difference between revisions

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'''Chromosome 2q 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 2]]. The severity of the condition and the signs and symptoms depend on the size and location of the [[Genetic deletion|deletion]], and which [[gene]]s are involved. Features that often occur in people with chromosome 2q deletion include [[developmental delay]], [[intellectual disability]], [[behavior problem]]s, and distinctive facial features.
'''Chromosome 2q 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 2]]. The severity of the condition and the signs and symptoms depend on the size and location of the [[Genetic deletion|deletion]], and which [[gene]]s are involved. Features that often occur in people with chromosome 2q deletion include [[developmental delay]], [[intellectual disability]], [[behavior problem]]s, and distinctive facial features.

Revision as of 03:42, 1 June 2020

Chromosome 2q 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 2. 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 2q deletion include developmental delay, intellectual disability, behavior 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.[1]

See also

References

  1. ^ "Chromosome 2q deletion - Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 12 August 2017.Public Domain This article incorporates text from this source, which is in the public domain.