Diagnostic test
FISH FOR DELETION 22Q SYNDROME /CATCH 22 - (Outlab)
About test
What does FISH FOR DELETION 22Q SYNDROME /CATCH 22 - (Outlab) measure?
This FISH test looks for a missing segment of genetic material in the 22q region of chromosome 22, associated with 22q deletion (CATCH 22) syndromes. It may be used when a healthcare professional is evaluating features or family history that could be linked to this chromosomal change. Results are interpreted alongside clinical findings, family history, and other relevant genetic tests.
This overview is educational. Use the recorded preparation, sample and lab-partner details below for collection guidance, and confirm any missing information before collection.
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Prices, report times and availability are shown from the catalog records for each eligible partner.
Thyrocare
- Sample for analysis
- Confirm with the collection team
- Report time
- To be confirmed
Preparation and specimen requirements can vary by test and laboratory. Follow the instructions shown for your selected partner and any advice from your healthcare professional.