InfantGen Scan
Ensure your baby’s health with advanced genetic screening
INFANTGEN SCAN provides a comprehensive analysis of your baby's genetic profile. Gain insights into potential health conditions early.
Explore Your Baby’s Genetic Health with Precision Using Our Advanced INFANTGEN SCAN, Offering Early Detection of Genetic Conditions
Test Advantages
Accurate and reliable results
Proactive health management
Informed health decisions
Early detection of potential conditions
InfantGen Scan
The INFANTGEN SCAN at Genome X is a state-of-the-art, non-invasive test designed to provide a thorough analysis of your baby’s genetic profile. This test offers valuable insights into potential health conditions by examining genetic markers, helping you understand your baby’s genetic risks early on. With detailed and accurate results, this test supports proactive health management and ensures you can make informed decisions regarding your baby’s well-being.
Experience the Future of Genetic Testing with Our State-of-the-Art Solutions, Delivering Accurate Results and Comprehensive Support
Deletions
Duplications
This test offers early genetic insights into your infant's health by identifying specific genetic anomalies through a simple sample. It provides valuable information on deletions and duplications, helping in the early detection of potential genetic conditions.
Infant Gen Scan (Basic) offers a detailed genetic analysis to detect:
Deletions and Duplications
Autosomal Recessive Metabolic Disorders
Wilson's Disease
Hearing Loss
CFTR-Related Conditions
This test provides crucial insights into your infant’s genetic health by identifying specific genetic anomalies and conditions, enabling early diagnosis and intervention
Infant Gen Scan (Premium) offers an extensive genetic analysis to detect:
Deletions and Duplications
Autosomal Recessive Metabolic Disorders
Wilson's Disease
Hearing Loss
CFTR-Related Conditions
32 X-linked Dominant and Autosomal Dominant Disorders, including:
Achondroplasia
Noonan Syndrome
X-linked Alport Syndrome
This comprehensive test provides a thorough evaluation of your infant’s genetic health, identifying a wide range of genetic conditions and enabling early diagnosis and targeted care.
Test Procedure
Genome X Test Procedure
A simple blood or saliva sample is collected from both partners.
Our lab uses advanced genetic sequencing technologies.
The samples are securely shipped to our laboratory.
Comprehensive genetic tests are conducted.
You receive a detailed report explaining the findings.
Key Features
Genome X Test Features
Swift Results
Test results delivered within 5 to 7 working days, ensuring top-notch service and accuracy.
Affordance
High-quality genetic testing made affordable, offering transparent pricing and exceptional value.
Reliable Results
High quality testing achieved through international collaborations to ensure precision and global expertise.
Confidential
Testimonials
Our Patients Reviews
"The genetic testing was accurate and fast—really impressed with the level of detail provided. Excellent service!"
