FISH can be used to confirm the diagnosis of specific chromosomal syndromes
Fluorescence in-situ hybridisation (FISH) can be used in conjunction with conventional or microarray analysis for the investigation of specific chromosomal syndromes. Available tests are listed below.
The suspected clinical condition for which testing is being sought must be included on the request form.
Targeted FISH for neonatal diagnosis of aneuploidy
For neonatal diagnosis of suspected chromosomal syndromes
Chromosomes X , Y, 13, 18 and 21
FISH
2 days
If not MBS eligible, please contact 1800 822 999 for pricing details
Standard pathology request form
Blood
Min 1mL in 1 x paediatric Lithium heparin tube
Test is performed with conventional chromosome analysis. No additional sample required.
