SDHD Gene Cowden Syndrome Type 3 NGS Genetic DNA Test
Introduction
The SDHD Gene Cowden Syndrome Type 3 NGS Genetic DNA Test is an advanced diagnostic tool designed to detect mutations in the SDHD gene, which is associated with Cowden syndrome, a genetic condition that increases the risk of certain cancers. This test employs Next Generation Sequencing (NGS) technology to provide precise genetic information, enabling healthcare providers to offer tailored medical advice and interventions.
What the Test Measures
This genetic test specifically measures alterations in the SDHD gene, which can indicate a predisposition to various tumors, particularly in the thyroid, breast, and other tissues. By identifying these mutations, the test can help in assessing the risk of developing associated cancers.
Who Should Consider This Test?
Individuals with a family history of Cowden syndrome or related cancers should consider undergoing the SDHD Gene Cowden Syndrome Type 3 NGS Genetic DNA Test. Symptoms may include:
- Multiple hamartomas (benign tumors)
- Thyroid abnormalities
- Breast cancer
- Gastrointestinal tumors
Additionally, individuals with known mutations in family members should also seek testing for comprehensive risk assessment.
Benefits of Taking the Test
- Early detection of genetic predispositions to cancer.
- Informed decision-making regarding screening and preventive measures.
- Personalized healthcare strategies based on genetic findings.
- Support for family members who may also be at risk.
Understanding Your Results
Results from the SDHD Gene Cowden Syndrome Type 3 NGS Genetic DNA Test will provide insights into whether you carry mutations associated with Cowden syndrome. A genetic counselor will assist in interpreting the results, discussing implications for your health and that of your family, and advising on potential surveillance and management options.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SDHD Gene Cowden Syndrome Type 3 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
The turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by Cowden syndrome.
Book Your Test Today!
We have branches across Kenya, including Nairobi, Mombasa, and Kisumu, to serve you better. For home sample collection services or to book your test, please call or WhatsApp us at +254711564616.
