CUL7 Gene Three M Syndrome Type 1 NGS Genetic DNA Test
Introduction
The CUL7 Gene Three M Syndrome Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to identify genetic mutations associated with Three M Syndrome. This condition is characterized by distinct physical features and developmental delays. Early detection through this test can significantly enhance patient management and family planning.
What the Test Measures
This test specifically measures mutations in the CUL7 gene, which are known to be linked to dysmorphology. By analyzing the genetic material, healthcare providers can better understand the underlying causes of developmental disorders in affected individuals.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Unusual physical features
- Growth delays
- Developmental delays
- Family history of genetic disorders
are encouraged to consider this test. Additionally, parents who have children with developmental concerns may benefit from genetic counseling and testing.
Benefits of Taking the Test
- Accurate diagnosis of genetic conditions
- Informed family planning decisions
- Access to targeted therapies and interventions
- Peace of mind through understanding genetic risks
Understanding Your Results
Results from the CUL7 Gene Three M Syndrome Type 1 NGS Genetic DNA Test will be interpreted by qualified genetic counselors and specialists. They will provide guidance on the implications of the results, potential next steps, and available resources for management and support.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 400,000 |
Regular Price | 560,000 |
Book the Test
To book the CUL7 Gene Three M Syndrome Type 1 NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to schedule an appointment. Our team is here to assist you with any inquiries and guide you through the testing process.
Turnaround time for results is approximately 3 to 4 weeks. The sample type required is either blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a genetic counseling session is recommended to discuss the clinical history and draw a pedigree chart of affected family members.
Don’t wait to uncover the genetic factors that may impact your health or your family’s health. Book your test today!