FAQs
How do I place an order?
What payment methods do you accept?
How long does shipping take?
What is your return policy?
Do you ship internationally?
Pediatric Comprehensive
Towards a future of proactive, personalized pediatric care
Unravel the Puzzle of Your Child's Health
Understand your child’s health on a genetic level by identifying their health risks in the early stages of life
Order Now
Consult Our Expert
An NGS-based test for identifying genetic risk factors associated with developing inherited disorders in the pediatric population.
- Early detection and risk prediction
- In-depth information on genetic variants
- Allows timely intervention to prevent complications
- Enables lifestyle changes to achieve the best health outcomes
Conditions / Disorders Covered:
Metabolic disorders
Hormonal/Endocrine Disorders
Blood Disorders/ Haemoglobinopathies
Cardiac Conditions
Immunodeficiency Conditions
Epilepsy
Other Neurological Disorders
Pediatric Cancers
Who Should Get Tested?
Essential for:
ALL
Kids Under 16 years
Especially for Patients with:
Premature babies
Babies with low birth-weight
Babies/children with a family history of genetic disorders
Children (0-16 years old)
Order Now
Consult Our Expert
Benefits of DGx Pediatric Comprehensive Test
- Reduces diagnosis and treatment time
- Confirms diagnosis for genetic disorders
- Informs on treatment and management strategies
What makes DGx Pediatric Comprehensive Test Special?
- Expanded screening panel
- Increased diagnostic power
- Rapid diagnosis
- Improved sensitivity and specificity
- Cost-effective
- Actionable and easy-to-interpret reports
Test Specifications
Specimen required:
4ml EDTA-Blood
Sequencing coverage:
>99.0% >20X
No. of genes covered:
450+
Variant types covered:
SNPs, indels
Turnaround time:
21 Days
Guidelines followed:
ACMG & AMP
