Nx Gen Sequencing Dementia Test
Introduction
The Nx Gen Sequencing Dementia Test is an advanced genetic test aimed at identifying mutations that may contribute to the development of dementia. This test is crucial for individuals with a family history of dementia or those experiencing symptoms of cognitive decline. By utilizing next-generation sequencing (NGS) and Sanger sequencing methods, this test provides an in-depth analysis of various genetic markers associated with dementia.
What the Test Measures
This test analyzes multiple genes known to be linked to dementia, including:
- APOE
- APP
- CHMP2B
- CSF1R
- FUS
- GRN
- MAPT
- PRNP
- PSEN1
- PSEN2
- SORL1
- TARDBP
- TREM2
- UBE3A
- VCP
By identifying these genetic variants, the test helps in assessing the risk of developing dementia-related disorders.
Who Should Consider This Test?
This test is recommended for individuals who:
- Have a family history of dementia
- Are experiencing early signs of cognitive decline
- Have risk factors such as age, lifestyle, or other health conditions
Benefits of Taking the Test
The Nx Gen Sequencing Dementia Test offers several benefits:
- Identifies genetic predispositions to dementia, enabling early intervention.
- Provides peace of mind for individuals concerned about their cognitive health.
- Guides healthcare providers in creating personalized management plans.
- Empowers patients to make informed decisions about their health.
Understanding Your Results
Upon receiving your results, it is essential to consult with a healthcare professional, preferably a neurologist, who can help interpret the findings and discuss potential next steps. Understanding your genetic risk can be a powerful tool in managing your health.
Test Pricing
Price Type | Amount (NGN) |
---|---|
Discount Price | 468,000 NGN |
Regular Price | 520,000 NGN |
How to Book the Test
To book the Nx Gen Sequencing Dementia Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and answer any questions you may have.
Test Details
Turnaround Time: Sample Daily by 9 am; Report in 40 Working Days
Sample Type: Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes. Ship refrigerated. DO NOT FREEZE. Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Pre-test Instructions: Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory.
Specialty: Neurologist
Department: Molecular Diagnostics
Method: NGS, Sanger Sequencing
Disease Type: Genetic Disorders – Dementia