KIAA0586 Gene Joubert Syndrome Type 23 NGS Genetic DNA Test
Introduction to the Test
The KIAA0586 Gene Joubert Syndrome Type 23 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with Joubert syndrome, a rare neurological disorder. This test employs Next Generation Sequencing (NGS) technology to provide a comprehensive analysis of the KIAA0586 gene, which plays a critical role in brain development.
What the Test Measures
This genetic test detects mutations in the KIAA0586 gene that may lead to Joubert syndrome. By analyzing DNA samples, the test can identify specific genetic variations that are associated with this condition, helping to confirm a diagnosis and guide treatment options.
Who Should Consider This Test?
Individuals who exhibit symptoms of Joubert syndrome, such as developmental delays, ataxia, and abnormal eye movements, should consider this test. Additionally, those with a family history of neurological disorders or genetic conditions may benefit from genetic counseling and testing.
Benefits of Taking the Test
- Provides clarity on genetic causes of neurological symptoms.
- Facilitates early diagnosis and intervention.
- Informs family planning and genetic counseling options.
- Helps in understanding the prognosis and potential treatment pathways.
Understanding Your Results
Once the test is completed, results will be analyzed by a team of genetic specialists. A genetic counselor will help interpret the findings, discussing the implications of any identified mutations and suggesting further steps based on the results.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
KIAA0586 Gene Joubert Syndrome Type 23 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across all major cities in Kenya, providing convenient access to our diagnostic services. You can also opt for home sample collection for your convenience. To book the KIAA0586 Gene Joubert Syndrome Type 23 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616 today!
Test Details
- 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 undergoing the test is required, along with a genetic counseling session to draw a pedigree chart of affected family members.
- Specialty: Neurologist
- Department: Genetics
- Method: NGS Technology
- Disease Type: Neurological Disorders