DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test
Introduction
The DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the DCLRE1C gene. This test plays a vital role in the early diagnosis and management of Omenn syndrome, a rare immunological disorder characterized by a combination of severe combined immunodeficiency and eczema.
What the Test Measures
This genetic test specifically measures and detects mutations in the DCLRE1C gene, which is essential for the development and function of immune cells. Identifying these mutations can help in diagnosing Omenn syndrome and related immunological disorders.
Who Should Consider This Test?
Individuals who should consider the DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test include:
- Patients exhibiting symptoms of immunodeficiency, such as recurrent infections.
- Individuals with a family history of Omenn syndrome or other immunological disorders.
- Patients with eczema and lymphadenopathy that are unexplained by other conditions.
Benefits of Taking the Test
The DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test offers numerous benefits, including:
- Early and accurate diagnosis of Omenn syndrome.
- Informed treatment decisions based on genetic insights.
- Better management of symptoms and associated health risks.
- Guidance for family planning and understanding hereditary risks.
Understanding Your Results
Upon receiving your test results, it is essential to consult with a healthcare professional who specializes in genetics. They will help interpret the findings and discuss potential implications for your health and family.
Test Details
| Test Name | Price (NGN) |
|---|---|
| DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test | Regular Price: 560,000 NGN |
| Discount Price | 400,000 NGN |
Booking the Test
To book the DCLRE1C Gene Omenn Syndrome NGS Genetic DNA Test, please contact us at +2348077798758 via call or WhatsApp. Our team is ready to assist you with scheduling your appointment and providing necessary pre-test instructions, including a genetic counseling session to draw a pedigree chart of affected family members.
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 one drop of blood on an FTA card. It is important to provide a clinical history of the patient prior to testing.
Consult with a dermatologist or geneticist for further evaluation and guidance regarding this test.
