Brat1 Gene Neurodevelopmental Disorder With Cerebellar Atrophy And With Or Without Seizures Ngs Genetic Dna Test
Introduction
The Brat1 Gene Neurodevelopmental Disorder with Cerebellar Atrophy and with or without Seizures NGS Genetic DNA Test is a revolutionary diagnostic tool designed to identify genetic mutations associated with neurological disorders. This test utilizes Next-Generation Sequencing (NGS) technology to provide comprehensive insights into the genetic factors contributing to cerebellar atrophy and related conditions. Understanding these genetic components is crucial for effective diagnosis, management, and treatment planning for affected individuals.
What the Test Measures
This test specifically measures mutations in the BRAT1 gene, which are linked to neurological disorders characterized by cerebellar atrophy. By identifying these mutations, healthcare providers can better understand the underlying causes of symptoms and tailor treatment plans accordingly.
Who Should Consider This Test
Individuals who exhibit symptoms such as developmental delays, seizures, or coordination difficulties should consider undergoing this test. Additionally, families with a history of neurological disorders or those who have been advised by a neurologist may benefit significantly from this genetic assessment.
Benefits of Taking the Test
- Early detection of genetic predispositions to neurological disorders.
- Informed decision-making regarding treatment options and management strategies.
- Enhanced understanding of family health history and potential risks.
- Access to genetic counseling for affected families.
Understanding Your Results
Results from the Brat1 Gene Neurodevelopmental Disorder Test can provide valuable insights into the genetic factors influencing neurological health. A genetic counselor will help interpret the results and discuss the implications for treatment and family planning.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Brat1 Gene Neurodevelopmental Disorder Test | 40,000 KSh | 56,000 KSh |
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or even a single drop of blood on an FTA card. It is essential to provide a clinical history of the patient undergoing the test, and a genetic counseling session to draw a pedigree chart of family members affected by BRAT1 Gene Neurodevelopmental Disorder is recommended.
Book Your Test Today!
We have branches across Kenya, including major cities such as Nairobi, Mombasa, and Kisumu, and we offer home sample collection services for your convenience. To book the Brat1 Gene Neurodevelopmental Disorder Test, call or WhatsApp us at +254711564616.
