Chromosome 3q deletion

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Disease Overview

Chromosome 3q 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 3. 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 3q deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features.[9067] 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.


Synonyms

  • Deletion 3q
  • Monosomy 3q
  • 3q deletion
  • 3q monosomy
  • Partial monosomy 3q

For more information, visit GARD.

National Organization for Rare Disorders