|Prenatal Aneuploidy FISH||
Fluorescence in situ hybridization (FISH)
|Container Type||Container Size||Specimen Volume|
|N/A||5 mL-10 mL|
Room temperature - 24 hour(s)
- Do not add fixative
- Do not centrifuge
- Do not freeze
- Keep at room temperature
- Transport to laboratory as soon as possible
Reasons for Rejection
- Fixed specimen
- Frozen specimen
- Minimum volume/concentration not submitted
- Delayed or improper handling
Submission of a completed Prenatal Genetic Test Requisition Form is required. To request for the form, please call Cytogenetics Lab at (614) 722-5321.
This test evaluates for numerical abnormalities of chromosomes 13,18, X, and Y and is used to screen for common numerical chromosome abnormalities such as trisomy 13, trisomy 18, trisomy 21, monosomy X (Turner syndrome), triploidy and tetraploidy. This test is done by fluorsecence in situ hybridization (FISH) analysis performed on direct (uncultured) amniotic fluid specimen, and interphase cells present in the specimen will be analyzed. Because this test is a screening test, our laboratory does not offer this test as a stand-alone test; this test MUST be performed along with other cytogenetic test(s), such as amniotic fluid chromosome analysis and/or prenatal microarray analysis.
To perform this test, please submit 5 mL amniotic fluid in addition to the amniotic fluid volume required for other testing requested on the sample (e.g. additional 15-20 mL required for chromosome analysis or microarray analysis). Amniotic fluid should be collected in a non-toxic, sterile container and transported at room temperature.
- 88271 (x5)