Genetic screening for your baby





Genetic screening for your baby



Genetic screening for your baby


Banking your baby’s cord blood means you are already giving them the best possible start.


With newborn screening, you can access information that will also enable you to take steps to safeguard your baby’s health.

With BabyInsight you can screen your baby for a range of manageable conditions and sensitivities likely to develop within their first few months of life:

  • AAT deficiency
  • Gluten sensitivity
  • Lactose intolerance
  • Drug-induced deafness
  • Hereditary fructose intolerance


Cells4Life Baby Insight Genetic Screening

Safe and reliable
– Only £360


What is BabyInsight?

BabyInsight is an early detection DNA screen that can provide you with crucial information about your baby’s predisposition to certain conditions which manifest at a young age.

This allows you and your healthcare professional to make informed decisions before these conditions impact on your baby’s health and wellbeing. The test is carried out using a cheek swab sample, or a very small portion of the waste fraction of your baby’s cord blood.

Mother and baby cells4life

What conditions does BabyInsight screen for?

AAT Deficiency

AAT Deficiency

Alpha-1 antitrypsin (AAT) deficiency is a genetic condition that raises your risk for lung disease and other diseases.

Early identification of this condition can enable you to make lifestyle changes, like keeping your baby away from second-hand smoke, dust and fumes, which could exacerbate their risk.

Gluten Sensitivity

Gluten Sensitivity

Coeliac disease is a condition where your immune system attacks your own tissues when you eat gluten. It limits the absorption of nutrients.

Early screening for Gluten sensitivity helps guide which foods your baby may need to avoid.

Lactose Intolerance

Lactose Intolerance

Lactose intolerance is a common digestive problem where the body is unable to digest lactose, a type of sugar mainly found in milk and dairy products.

As with Gluten sensitivity, an early screen for intolerance of lactose will help steer you and your baby’s healthcare professional on what food you may need to be more cautious with.  

Drug-Induced deafness

Drug-Induced Deafness

Drugs that cause hearing loss are directly toxic to the inner ear or auditory nerve, leading to sensorineural deafness. Drug ototoxicity is dependent on the dose and duration of exposure.

BabyInsight screens for genetic predisposition to this condition, enabling your doctor to be selective about any drugs your child may need if they are at risk.

Hereditary fructose intolerance

Hereditary Fructose Intolerance

Hereditary fructose intolerance (HFI) is a metabolic disease caused by the absence of an enzyme called aldolase B. In people with HFI, ingestion of fructose and sucrose causes severe hypoglycemia (low blood sugar) and the build up of dangerous substances in the liver.

Through screening you may discover if there are foods to avoid which could negatively impact your baby’s health.


Postnatal screening – what’s involved

Order Baby Insight genetic screening

Request your BabyInsight

Select the BabyInsight option when you book your cord blood banking service, indicating whether you would prefer a mouth swab or to use a tiny portion of cord blood for the test.

Genetic Screening Sampling

Collection on the day

The BabyInsight collection process is quick, simple and safe, whether you choose to do it alongside cord blood collection or later, as a standalone service. Simply swab the inside of your baby’s cheek for 30 seconds before sealing and sending your sample to us for analysis.

Genetic Screening Results

Your results

Your baby’s sample will be tested against the 5 main conditions we test for within 7 days of receipt. We will contact you with the results as soon as they are available, which usually takes around 4 weeks.


Connect with us

Pin It on Pinterest