MED12 Gene Lujan-Fryns Syndrome NGS Genetic DNA Test
Introduction
The MED12 Gene Lujan-Fryns Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the MED12 gene, which are linked to Lujan-Fryns syndrome. This genetic disorder is characterized by a range of developmental and physical anomalies, and understanding its genetic basis is crucial for effective management and family planning.
What the Test Measures
This test measures specific mutations in the MED12 gene, providing insights into the genetic factors that contribute to Lujan-Fryns syndrome. By analyzing the DNA, healthcare providers can determine the likelihood of the syndrome being passed on to future generations.
Who Should Consider This Test?
Individuals or families with a history of:
- Developmental delays
- Physical anomalies
- Genetic disorders
should consider this test. A genetic counseling session is recommended prior to testing to discuss family history and draw a pedigree chart of affected members.
Benefits of Taking the Test
- Identifies genetic risks associated with Lujan-Fryns syndrome.
- Informs family planning decisions.
- Guides management and treatment options for affected individuals.
- Provides peace of mind through understanding genetic health.
Understanding Your Results
Once the results are available, typically within 3 to 4 weeks, our genetic counselors will help interpret the findings. Understanding the implications of your genetic test results is essential for making informed health decisions.
Test Name and Price
| Discount Price | Regular Price |
|---|---|
| 40,000 KSh | 56,000 KSh |
Our Services
We have branches across major cities in Kenya, including Nairobi, Mombasa, and Kisumu. We also offer home sample collection services for your convenience.
Book the Test Today!
Don’t wait! Understanding your genetic health is critical. Call or WhatsApp us at +254711564616 to book your MED12 Gene Lujan-Fryns Syndrome NGS Genetic DNA Test today!
