Because Every Baby Deserves a Healthy Start
In the first days of life, your baby’s body is developing rapidly — and early detection can make a lifetime of difference. The Neonatal Genomic Test is a powerful tool that screens your newborn for hundreds of rare genetic conditions, even before symptoms appear.
What Is It?
A simple test using a few drops of blood or a cheek swab can uncover genetic changes linked to:
- Metabolic disorders
- Immune system deficiencies
- Neurological and developmental conditions
- Hereditary diseases treatable if caught early
Why It Matters
Non-invasive & Safe – Done shortly after birth
Early Diagnosis = Early Action – Many conditions can be managed or even prevented
Comprehensive Screening – Covers 200+ actionable genetic conditions
Personalized Care Plan – Results help guide your baby’s health from day one
For Every Baby, Not Just High-Risk
Even without a family history, some genetic conditions can occur unexpectedly. Neonatal Genomic Testing offers peace of mind and a stronger foundation for lifelong health.
For further information, Please contact us at: + 297 586 1600
