TSEN2 Gene Pontocerebellar Hypoplasia Type 2B Genetic Test
Are you or a loved one experiencing symptoms of pontocerebellar hypoplasia type 2B (PCH2B)? DNA Labs UAE offers a comprehensive genetic test to help diagnose this rare neurological disorder.
Test Name: TSEN2 Gene Pontocerebellar Hypoplasia Type 2B 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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information:
Before undergoing the TSEN2 Gene Pontocerebellar Hypoplasia Type 2B Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by PCH2B.
Test Details:
The TSEN2 gene is associated with pontocerebellar hypoplasia type 2B (PCH2B), a progressive neurological disorder characterized by underdevelopment of the pons and cerebellum. These brain regions are responsible for motor control and coordination.
NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously. In the case of PCH2B, NGS testing can identify mutations or variants in the TSEN2 gene linked to the disorder. This information confirms the diagnosis of PCH2B and provides insights into the specific genetic variant causing the condition.
NGS genetic testing is valuable for genetic counseling, prognosis, and potential treatment options. However, it may not be available at all healthcare facilities and may require a referral to a specialized genetic testing laboratory. It is crucial to undergo genetic testing under the guidance of a healthcare professional specializing in genetics, such as a genetic counselor or medical geneticist.
Don’t let the symptoms of PCH2B go undiagnosed. Contact DNA Labs UAE today to schedule your TSEN2 Gene Pontocerebellar Hypoplasia Type 2B Genetic Test and gain valuable insights into your condition.
| Test Name | TSEN2 Gene Pontocerebellar hypoplasia type 2B Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for TSEN2 Gene Pontocerebellar hypoplasia type 2B NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TSEN2 Gene Pontocerebellar hypoplasia type 2B |
| Test Details |
The TSEN2 gene is associated with a rare genetic disorder called pontocerebellar hypoplasia type 2B (PCH2B). PCH2B is a progressive neurological disorder characterized by underdevelopment (hypoplasia) of the pons and cerebellum, which are parts of the brain involved in motor control and coordination. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of PCH2B, NGS genetic testing can be used to identify mutations or variants in the TSEN2 gene that are associated with the disorder. By analyzing the TSEN2 gene, NGS testing can help confirm a diagnosis of PCH2B and provide information about the specific genetic variant causing the condition. This information can be useful for genetic counseling, prognosis, and potential treatment options. It’s important to note that NGS genetic testing may not be available at all healthcare facilities and may require a referral to a specialized genetic testing laboratory. Additionally, genetic testing should be done under the guidance of a healthcare professional who specializes in genetics, such as a genetic counselor or medical geneticist. |
