Genetic Testing Enquiry Form
Pediatric Screening
Towards a future of proactive, personalized pediatric care
Genetic Testing for Children & Inherited Disorders■
Understand your child’s health on a genetic level by identifying their health risks in the early stages of life
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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
Inherited Conditions We Screen For
Metabolic disorders
Hormonal/Endocrine Disorders
Blood Disorders/ Haemoglobinopathies
Cardiac Conditions
Immunodeficiency Conditions
Epilepsy
Other Neurological Disorders
Pediatric Cancers
Who Should Take the DGx Pediatric Screening Test?
Who Should Take the DGx Pediatric Screening Test?
Essential for:
ALL
Kids Under 18 years
Especially for Patients with:
✦ Premature babies
✦ Babies with low birth-weight
✦ Babies/children with a family history of genetic disorders
✦ Children (0-18 years old)
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Benefits of DGx Pediatric Screening test
- Reduces diagnosis and treatment time
- Confirms diagnosis for genetic disorders
- Informs on treatment and management strategies
What Makes DGx Pediatric Screening Different?
- Expanded screening panel
- Increased diagnostic power
- Rapid diagnosis
- Improved sensitivity and specificity
- Cost-effective
- Actionable and easy-to-interpret reports
DGx Pediatric Screening — Test Specifications
Specimen required:
4ml EDTA-Blood
Sequencing coverage:
>99.0% >20X
No. of genes covered:
450+
Variant types covered:
SNPs, indels
Turnaround time:
28 Days
Guidelines followed:
ACMG & AMP
