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.[citation needed]
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
editReferences
edit- ^ "Chromosome 2q deletion - Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 12 August 2017.
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