Fluorescent In Situ Hybridisation

FISH Overview

FISH or Fluorescent In Situ Hybridisation assesses the presence of an abnormal number of chromosomes. It is a diagnostic test that is often performed in conjunction with other cytogenetic tests.

FISH
helps prospective parents in more ways than one

Provides a targeted and rapid diagnosis of chromosomal abnormalities

Allows you to begin planning for a child with special needs or make a decision about carrying the child to term

Ensures comprehensive results in just 48 hours.

Provides Free Genetic Counselling

How Does FISH Work?

Order:

A doctor places an order for the test

Sample Collection:

The sample is collected and shipped to the lab

Testing:

Reports are shared within 48 Hours

Post-test counselling

This test also offers complimentary genetic counselling in order to understand results better

Make an intelligent life decision for your child with

FISH

Please note that FISH can only be ordered by a physician. They would also be the only person to receive your results and will pass them along to you. If you are unable to find a physician, contact us on 1800-266-5533 & we will organise one for you at no additional cost.

Frequently Asked Questions

Down syndrome (Trisomie 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Turner syndrome (Monosomy X)
Klinefelter syndrome (XXY)
Jacobs syndrome (XYY)
Triple X syndrome (XXX)
Turner Syndrome ( A female baby with a missing or damaged XX chromosome)

The sample requirements for this test include:

Chorionic villus sampling (CVS). - This includes obtaining a small sample of the baby’s cells from the chorionic villi, which are placental tissues.
Amniocentesis - This includes obtaining a sample of the amniotic fluid, or the liquid that surrounds your baby in the womb.