SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 Genetic Test
At DNA Labs UAE, we offer the SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 Genetic Test. This test is designed to diagnose and provide information about the SLC52A2 gene, which is associated with Brown-Vialetto-Van Laere syndrome type 2 (BVVLS2). BVVLS2 is a rare neurological disorder characterized by progressive hearing loss, cranial nerve palsies, and respiratory problems.
Test Details
The SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 Genetic Test is conducted using NGS (Next-Generation Sequencing) Technology. This type of genetic testing allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of BVVLS2, this test involves sequencing the SLC52A2 gene to identify any mutations or variations that may be causing the syndrome.
Components
- Test Name: SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 Genetic Test
- 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
Prior to undergoing the SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 Genetic Test, it is important to provide the clinical history of the patient. A Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with BVVLS2 and gather relevant information.
Test Benefits
This genetic test can help confirm a diagnosis of BVVLS2 and provide information about the specific mutation in the SLC52A2 gene. It can also be used for carrier testing in families with a history of the syndrome and for genetic counseling.
It is crucial to note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support.
| Test Name | SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 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 SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test gene SLC52A2 |
| Test Details |
The SLC52A2 gene is associated with Brown-Vialetto-Van Laere syndrome type 2 (BVVLS2). BVVLS is a rare neurological disorder characterized by progressive hearing loss, cranial nerve palsies, and respiratory problems. BVVLS2 specifically refers to cases caused by mutations in the SLC52A2 gene. NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of BVVLS2, an NGS genetic test would involve sequencing the SLC52A2 gene to identify any mutations or variations that may be causing the syndrome. This genetic test can help confirm a diagnosis of BVVLS2 and provide information about the specific mutation in the SLC52A2 gene. It can also be used for carrier testing in families with a history of the syndrome and for genetic counseling. It is important to note that genetic testing should always be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support. |
