Maternal UPD Chr 14 Gene Temple Syndrome NGS Genetic DNA Test
Introduction
The Maternal UPD Chr 14 Gene Temple Syndrome NGS Genetic DNA Test is a specialized genetic test designed to identify maternal uniparental disomy (UPD) of chromosome 14. This condition is associated with various genetic disorders including Temple syndrome, which can lead to significant developmental and health issues. Understanding the implications of this test is crucial for families, especially those with a history of genetic disorders.
What the Test Measures
This test detects the presence of maternal UPD on chromosome 14, which occurs when both copies of a chromosome are inherited from the mother, leading to an imbalance in gene expression. It utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results.
Who Should Consider This Test
Individuals or families with a history of:
- Genetic disorders
- Unexplained developmental delays
- Growth abnormalities
- Family history of Temple syndrome
should consider this test. Symptoms such as growth retardation, obesity, and distinctive facial features may prompt the need for testing.
Benefits of Taking the Test
- Early diagnosis of genetic conditions to allow for timely intervention.
- Informed family planning based on genetic risk assessment.
- Access to tailored medical care and support.
Understanding Your Results
Results from the Maternal UPD Chr 14 Gene Temple Syndrome NGS Genetic DNA Test will provide insights into whether maternal UPD is present. A genetic counselor will help interpret the results, discussing potential implications for health and development.
Test Details and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Maternal UPD Chr 14 Gene Temple Syndrome NGS Genetic DNA Test | 400,000 | 560,000 |
How to Book the Test
To book the Maternal UPD Chr 14 Gene Temple Syndrome NGS Genetic DNA Test or for more information, please call or WhatsApp us at +2348077798758. Our team is ready to assist you with any inquiries.
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 going for the test is required, along with a genetic counseling session to draw a pedigree chart of family members affected by the condition.
