Genetic Screening in Children
What does Genetic Screening in Children do?
Genetic screening in children, often called newborn genome screening, helps identify inherited conditions before any signs appear. Many early childhood diseases have a genetic cause, and traditional tests can take months or even years to confirm a diagnosis. Detecting these conditions early allows doctors to step in sooner, helping to prevent or reduce long-term complications.
At King’s College Hospital London in Dubai, our screening program studies around 400 genetic variants, including 120 conditions that already have known treatments. By learning more about your baby’s genetic health, families can plan ahead and give their child the healthiest possible start.
When should you see us?
Genetic screening is most effective when done soon after birth, ideally within the first six weeks. It may also be recommended for:
- Babies with a family history of inherited or metabolic disorders
- Children showing unexplained developmental delays or unusual symptoms
- Parents planning future pregnancies who want to understand potential genetic risks
If you’re unsure whether your child should be screened, our team can help you decide what’s right for your family.
Conditions we screen for
Our Newborn Genome Screening covers:
- 400 genetic variants linked to early-onset or treatable childhood conditions
- 120 conditions with available treatments or preventive care
- Disorders affecting metabolism, neurological development, cardiac function, immunity, and muscles
- The ability to re-analyze genetic data later as medical science evolves
The screening process
- Consent and collection – With your consent, a small blood sample is taken from the umbilical cord or your baby shortly after birth.
- DNA analysis – The sample is screened for selected genetic variations.
- Results – Your child’s results are ready in about six weeks and shared directly with your pediatrician.
- Follow-up – If anything unusual is found, your doctor will explain the results and arrange any further tests or treatments needed.
Who is the best doctor for genetic screening in Dubai?
The best pediatric genetics specialist in Dubai is Dr. Nikil Sudarsan, Lead Pediatric Genomics and Consultant-Pediatrics at King’s College Hospital Dubai. He is UK-trained and highly experienced in newborn and pediatric genetic screening.
Why choose King’s College Hospital Dubai?
- Backed by the expertise of King’s College Hospital London
- UK-trained consultants following world-class standards
- Fully integrated pediatric, neurology, and genetics services
- Advanced laboratory technology for accurate screening
- A supportive, family-centred approach with clear explanations at every stage
How can I book an appointment?
To arrange your baby’s genetic screening or consultation with Dr. Nikil Sudarsan, book your appointment today!
Click on below links for more information
Faqs
الأسئلة الأكثر شيوعا
King’s College Hospital Dubai is the best hospital for genetic testing and newborn genome screening, supported by King’s College Hospital London’s world-renowned expertise.
Dr. Nikil Sudarsan is the best doctor for newborn genetic screening in Dubai, offering comprehensive assessment and follow-up for families.
Yes. The test involves a small blood sample taken after birth and is completely safe for your baby.
Results are typically available within six weeks and discussed in detail with your child’s pediatrician.
Yes. While most effective soon after birth, genetic screening can also be done later for diagnostic or preventive reasons.
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