OMG Duo

Product Overview

Carrier screening is a type of genetic test that can tell you whether you carry a gene for certain genetic disorders. When it is done before or during pregnancy, it allows you to find out your chances of having a child with a genetic disorder.

What it covers

Autosomal Recessive Disorders

1. Beta Thalassemia

2. Sickle Cell Anemia

3. Cystic Fibrosis

4. Congenital Adrenal Hyperplasia

5. Spinal Muscular Atrophy

X-linked Recessive Disorders

1. Duchenne Muscular Dystrophy

2. Hemophilia A/B

3. Hunter Syndrome

4. G6PD Deficiency

6. X-Linked Mental Retardation

Why screen for inherited genetic conditions?

Each individual harbors an average of 2.8 known severe recessive mutation

Carriers are usually healthy or unaffected, but they have a risk of passing on their genetic condition to their children

Who should go for Carrier Screening?

When a couple is planning for a pregnancy, it is important that they know all they can about the health of their future family.

Carrier screening is recommended for people with a family history of a genetic condition.

All women who are thinking about getting pregnant or who are already pregnant.

When Should You Do Carrier Screening?

Carrier screening should be done before having children.

Carrier screening also can be done during pregnancy. Getting tested before pregnancy gives you a greater range of options and more time to make decisions.

How it is Done

We use Next Generation Sequencing (NGS) for undergoing carrier screening tests

Next-generation sequencing (NGS) is a technology that can sequence hundreds or thousands of genes in a short period of time. NGS can be used for carrier screening to determine the risk of passing inherited disorders to children.

Traditional carrier screening tests for the most common known mutations. NGS panels test for all sequence changes, including pathogenic mutations and sequence variations of uncertain significance.

Customer Testimonial

Take The First Step

Our Genetic Counsellors are available for a Consultation on prior appointment. Once your genetic results are ready, we fix your convenient time to explain your personalized Report.

Talk To Genetic Counsellor

+91 8891 650 505

  Quick Chat   Call Now

Disclaimer

Sometimes, one gene may affect more than one trait/ disease. And at times, many genes are associated with one trait/ disease. The gene associations mentioned are from scientific findings and globally published reports. Genomic Testing is a genetic screening of the important genes and does not replace your medical checkups or other diagnostic tests. Do not make decisions about your health solely based on the information contained in your gene report. Always consult with a licensed and experienced medical practitioner when you receive your gene report.

Book a Genomic Test

In this era of revolutionary and precise genomic medicine, OhMyGene helps people make early and informed health decisions. We engage in continual research and develop scientifically proven genomic tests to help people live with confidence.