Baby Gender

Baby Gender helps your patients achieve their family balancing goals.

24-hour reporting using advanced NGS technology.

Result is 99% accurate.

CAP Accreditated.

What is Baby Gender test?

> Baby Gender test is used alongside in-vitro fertilization (IVF) to screen 5 most common abnormalities in embryos that is chromosome 21, 18, 13, X and Y.

> The abnormalities are identified as chromosome 21 – Down Syndrome, 18 – Edwards Syndrome, 13 – Patau Syndrome.

> The information obtained also provides the details of the gender of the embryo prior to transfer to help couples fulfil their family planning desires.

What is the procedure?

 

Why use Baby Gender test?

We use the most advanced technology, NGS (Next-Generation Sequencing) to perform the Baby Gender test:

> Rapid technology allowing embryos to be transferred in fresh (Day 3 embryos)

> Our technology and experience allows to analyze 5 most critical chromosomes 21, 18, 13, X and Y in a 12-hour procedure which provides results in more than 99% of cases.

> Most accurate determination of gender of the embryos along with higher pregnancy success rate as it eradicates the leading cause of the IVF Failure (chromosomal abnormality)

Who should use Baby Gender test?

> it is indicated for couples who wish to know the gender of their baby.

> Female patients over age 35

> Patients interested in selecting the best embryo for an elective Single Embryo Transfer or SET and avoid multiple pregnancies

> Patients who already have a child with a chromosomal abnormality or had a previous pregnancy with a chromosomal abnormality issue

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