PRNP Gene Huntington disease-like type 1 Genetic Test
Test Name: PRNP Gene Huntington disease-like type 1 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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: Clinical History of Patient who is going for PRNP Gene Huntington disease-like type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRNP Gene Huntington disease-like type 1.
Test Details
The PRNP gene Huntington disease-like type 1 NGS genetic test is a diagnostic test that analyzes the PRNP gene for specific genetic variants associated with Huntington disease-like type 1 (HDL1). HDL1 is a rare neurodegenerative disorder that shares some similarities with Huntington’s disease.
The test uses next-generation sequencing (NGS) technology to examine the entire PRNP gene, which provides instructions for the production of the prion protein. Mutations in the PRNP gene have been linked to various prion diseases, including HDL1. By analyzing the PRNP gene, this genetic test can identify specific variants that are known to cause HDL1. These variants disrupt the normal function of the prion protein, leading to the accumulation of abnormal proteins in the brain and subsequent neurodegeneration.
The test is typically performed on individuals who have symptoms consistent with HDL1 or have a family history of the disease. It can help confirm a diagnosis, guide treatment decisions, and provide important information for family planning. It’s important to note that this test specifically targets HDL1 and does not analyze other genes associated with Huntington’s disease or other types of Huntington disease-like disorders. Different genetic tests may be required to investigate other forms of these conditions.
Genetic testing for HDL1 can be conducted using a blood sample or other tissue samples. The samples are sent to a specialized laboratory where the DNA is extracted, and the PRNP gene is sequenced using NGS technology. The resulting genetic data is then analyzed to identify any disease-causing variants.
It is important to consult with a healthcare professional or a genetic counselor before undergoing genetic testing. They can provide guidance on the appropriateness of the test, explain the potential implications of the results, and help individuals understand the inheritance pattern of HDL1.
| Test Name | PRNP Gene Huntington disease-like type 1 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 PRNP Gene Huntington disease-like type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PRNP Gene Huntington disease-like type 1 |
| Test Details | The PRNP gene Huntington disease-like type 1 NGS genetic test is a diagnostic test that analyzes the PRNP gene for specific genetic variants associated with Huntington disease-like type 1 (HDL1). HDL1 is a rare neurodegenerative disorder that shares some similarities with Huntington’s disease. The test uses next-generation sequencing (NGS) technology to examine the entire PRNP gene, which provides instructions for the production of the prion protein. Mutations in the PRNP gene have been linked to various prion diseases, including HDL1. By analyzing the PRNP gene, this genetic test can identify specific variants that are known to cause HDL1. These variants disrupt the normal function of the prion protein, leading to the accumulation of abnormal proteins in the brain and subsequent neurodegeneration. The test is typically performed on individuals who have symptoms consistent with HDL1 or have a family history of the disease. It can help confirm a diagnosis, guide treatment decisions, and provide important information for family planning. It’s important to note that this test specifically targets HDL1 and does not analyze other genes associated with Huntington’s disease or other types of Huntington disease-like disorders. Different genetic tests may be required to investigate other forms of these conditions. Genetic testing for HDL1 can be conducted using a blood sample or other tissue samples. The samples are sent to a specialized laboratory where the DNA is extracted, and the PRNP gene is sequenced using NGS technology. The resulting genetic data is then analyzed to identify any disease-causing variants. It is important to consult with a healthcare professional or a genetic counselor before undergoing genetic testing. They can provide guidance on the appropriateness of the test, explain the potential implications of the results, and help individuals understand the inheritance pattern of HDL1. |
