GPSM2 Gene ChudleyMcCullough Syndrome NGS Genetic DNA Test
Introduction
The GPSM2 Gene ChudleyMcCullough Syndrome NGS Genetic DNA Test is an advanced genetic diagnostic tool designed to identify mutations in the GPSM2 gene, which are associated with Chudley-McCullough syndrome. This condition is characterized by a range of physical and developmental abnormalities. Understanding your genetic makeup can provide significant insights into health risks and guide effective management strategies.
What the Test Measures
This test specifically detects mutations in the GPSM2 gene, which plays a critical role in cellular processes. By identifying these mutations, healthcare providers can better understand the risk of developing Chudley-McCullough syndrome and related conditions.
Who Should Consider This Test?
Individuals who may benefit from this test include:
- Those with a family history of Chudley-McCullough syndrome.
- Patients presenting symptoms associated with dysmorphology.
- Individuals seeking genetic counseling for informed family planning.
Benefits of Taking the Test
Undergoing the GPSM2 Gene ChudleyMcCullough Syndrome NGS Genetic DNA Test offers numerous benefits:
- Accurate identification of genetic mutations.
- Informed decision-making regarding health management.
- Guidance for family planning and potential interventions.
- Access to tailored healthcare strategies based on genetic insights.
Understanding Your Results
Results from the GPSM2 Gene ChudleyMcCullough Syndrome NGS Genetic DNA Test will be provided in a detailed report, which will include:
- Identification of any detected mutations.
- Implications of the findings for health and family members.
- Recommendations for further action or testing if necessary.
Pricing Information
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| GPSM2 Gene ChudleyMcCullough Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the GPSM2 Gene ChudleyMcCullough Syndrome NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website for more details. Our team is ready to assist you with the booking process and any inquiries 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 is required, along with a genetic counseling session to draw a pedigree chart of family members affected by the GPSM2 gene.
Specialty: Pediatrics | Department: Genetics | Method: NGS Technology | Disease Type: Dysmorphology
