IGF1 Gene Growth Retardation with Deafness and Mental Retardation Due to IGF1 Deficiency NGS Genetic DNA Test
Introduction
The IGF1 Gene Growth Retardation with Deafness and Mental Retardation Due to IGF1 Deficiency NGS Genetic DNA Test is a crucial diagnostic tool designed to identify genetic abnormalities associated with significant developmental issues. This test is particularly relevant in the field of pediatrics, where early diagnosis can lead to timely interventions and improved outcomes for affected individuals.
What the Test Measures
This genetic test detects mutations in the IGF1 gene, which is linked to growth retardation, deafness, and cognitive impairments. By utilizing Next Generation Sequencing (NGS) technology, the test provides a comprehensive analysis of the genetic material, enabling clinicians to understand the underlying causes of these conditions.
Who Should Consider This Test
Individuals who exhibit symptoms such as:
- Growth retardation
- Hearing loss or deafness
- Cognitive delays or mental retardation
are encouraged to consider this test. Additionally, those with a family history of similar conditions may also benefit from genetic testing.
Benefits of Taking the Test
- Early identification of genetic disorders
- Informed decision-making regarding treatment options
- Understanding potential risks for family members
- Access to genetic counseling for better management
Understanding Your Results
Results from the IGF1 Gene Growth Retardation test will provide insights into whether a genetic mutation is present. A genetic counselor will assist in interpreting these results, discussing potential implications for treatment and family planning.
Test Pricing
| Discount Price | 400000 NGN |
|---|---|
| Regular Price | 560000 NGN |
How to Book the Test
To book the IGF1 Gene Growth Retardation with Deafness and Mental Retardation Due to IGF1 Deficiency NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient who is going for the test is necessary. A genetic counseling session to draw a pedigree chart of affected family members is also recommended.
This test falls under the specialty of Pediatrics, within the Genetics department, utilizing NGS technology to address dysmorphology concerns.
