A high-resolution cytogenetic tool to assess microlevel changes in the chromosome
Chromosomal MicroArray (CMA) Overview
The genetic material of humans is packed into small units called chromosomes that have their own genetic combinations. The slightest change in the genetic combination of these chromosomes– either addition, deletion, or an exchange – can result in birth defects, developmental delays, autism, and other health issues. The Chromosomal MicroArray is a high-resolution molecular genetic test that screens for such varied chromosomal DNA changes that may otherwise go undetected
When is the test recommended?
CMA testing is often recommended in the following scenarios:
- Multiple abnormalities which are not specific to a genetic syndrome
- Non-syndromic developmental delay or intellectual disability
- Autism Spectrum Disorders
Chromosomal MicroArray helps prospective parents in more ways than one
Provides a confirmed diagnosis for a series of chromosomal defect
Offers results in up to 10 days.
Allows you to begin planning for a child with special needs or make a decision about carrying the child to term.
Provides Genetic Counselling after the test to understand your results better.
How Does Chromosomal MicroArray Work?
Booking The Test
Your doctor places an order for the test.
Collection
Requires POC as a sample.
Laboratory Analysis
Testing and analysis is done in the lab.
Reports
The results are shared within 10 business days.
Counselling
Post-result counselling is offered to parents to understand the reasons behind the pregnancy loss and cope better.
Begin your healthy pregnancy journey with
Chromosomal MicroArray
Please note that Chromosomal MicroArray 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
