Chromosome 9q duplication
Alternate names[edit | edit source]
Duplication 9q; Trisomy 9q; 9q duplication; 9q trisomy; Partial trisomy 9q
Definition[edit | edit source]
Chromosome 9q duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the long arm (q) of chromosome 9.
Cause[edit | edit source]
This condition occurs when there is an extra copy of genetic material on the long arm (q) of chromosome 9.
Inheritance[edit | edit source]
Chromosome testing of both parents can provide more information on whether or not the duplication was inherited.
In most cases, parents do not have any chromosomal anomaly.
However, sometimes one parent is found to have a balanced translocation, where a piece of a chromosome has broken off and attached to another one with no gain or loss of genetic material.
- The balanced translocation normally does not cause any signs or symptoms, but it increases the risk for having an affected child with a chromosomal anomaly like a duplication.
Signs and symptoms[edit | edit source]
- The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved.
- Features that often occur in people with chromosome 9q duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features.
Diagnosis[edit | edit source]
Chromosome disorders may be suspected in people who have developmental delays, intellectual disabilities and/or physical abnormalities.
Several types of genetic tests can identify chromosome disorders:
- Karyotyping
- Microarray (also called array CGH)
- Fluorescence in situ hybridization (FISH)
Treatment[edit | edit source]
Treatment is based on the signs and symptoms present in each person.
NIH genetic and rare disease info[edit source]
Chromosome 9q duplication is a rare disease.
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