SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 Genetic Test
At DNA Labs UAE, we offer the SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 Genetic Test. This test is designed to analyze the SLC52A3 gene, which is associated with a rare genetic disorder known as Brown-Vialetto-Van Laere syndrome 1 (BVVL1).
Test Components and Price
The cost of the SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 Genetic Test is AED 4400.0. The test requires a sample of blood or extracted DNA, or just one drop of blood on an FTA Card.
Report Delivery and Method
Once the sample is received, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes.
Test Type and Doctor
The SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 Genetic Test falls under the category of Ear Nose Throat Disorders. It is recommended to consult with an ENT doctor for this test.
Test Department and Pre Test Information
The test is conducted in our Genetics department. Prior to the test, it is important to provide the clinical history of the patient who will be undergoing the SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. Additionally, a genetic counseling session may be conducted to create a pedigree chart of family members affected by the syndrome.
Test Details and Benefits
The SLC52A3 gene is associated with Brown-Vialetto-Van Laere syndrome 1, a rare genetic disorder characterized by progressive hearing loss, cranial nerve palsies, and respiratory problems. NGS genetic testing allows for the identification of mutations or variations in the SLC52A3 gene, aiding in diagnosis confirmation and understanding the genetic basis of the disorder. This information can be crucial for treatment and management options.
| Test Name | SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Ear Nose Throat Disorders |
| Doctor | ENT Doctor |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test gene SLC52A3 |
| Test Details |
The SLC52A3 gene is associated with a rare genetic disorder called Brown-Vialetto-Van Laere syndrome 1 (BVVL1). This syndrome is characterized by progressive hearing loss, cranial nerve palsies, and respiratory problems. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously and provide a comprehensive analysis of an individual’s genetic makeup. In the case of BVVL1, NGS genetic testing can be used to identify mutations or variations in the SLC52A3 gene that may be responsible for causing the syndrome. This can help in confirming a diagnosis, understanding the genetic basis of the disorder, and potentially providing information for treatment and management options. |
