WS1 Full Gene Sequence Analysis Wolfram Syndrome DIDMOAD
Introduction to the WS1 Full Gene Sequence Analysis
The WS1 Full Gene Sequence Analysis for Wolfram Syndrome (DIDMOAD) is a cutting-edge genetic test designed to identify mutations in the WFS1 gene. This test is crucial for diagnosing Wolfram Syndrome, a rare genetic disorder characterized by diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. Understanding your genetic predisposition can lead to early interventions and better management of the condition.
What the Test Measures
This test measures the complete sequence of the WFS1 gene. By analyzing the gene, healthcare providers can determine if there are any mutations that may lead to the development of Wolfram Syndrome.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Unexplained diabetes mellitus
- Vision problems
- Hearing loss
- Family history of Wolfram Syndrome
Additionally, those with risk factors or concerns about genetic conditions should consider this test. It is essential to consult with a healthcare provider to determine if this test is appropriate for your situation.
Benefits of Taking the Test
- Early diagnosis of Wolfram Syndrome can lead to better management of symptoms.
- Understanding your genetic makeup allows for personalized treatment options.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Once the test is completed, your healthcare provider will discuss the results with you. A positive result indicates a mutation in the WFS1 gene, which may lead to Wolfram Syndrome. Your doctor will guide you through the implications of your results and discuss potential next steps.
Test Details and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| WS1 Full Gene Sequence Analysis Wolfram Syndrome DIDMOAD | 720000 NGN | 960000 NGN |
How to Book the Test
To book the WS1 Full Gene Sequence Analysis for Wolfram Syndrome (DIDMOAD), please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Pre-Test Instructions
The WS1 Full Gene Sequence Analysis can be performed with a Doctor’s prescription. Please note that a prescription is not applicable for surgery and pregnancy cases or individuals planning to travel abroad.
Sample Type and Test Components
Sample types accepted include:
- Peripheral blood
- Amniotic Fluid
- Chorionic villi
- Cord blood
Test components include:
- Sterile container
- Sterile Normal Saline Container
- EDTA Vacutainer (2ml)
Turnaround Time
The expected turnaround time for the WS1 Full Gene Sequence Analysis is 4-6 weeks.
For more information or to book your test, please call or WhatsApp us at +2348077798758.
