Sale!

PRNP Gene Huntington Disease-like Type 1 Genetic Test

4,400 د.إ

-21%

The PRNP Gene Huntington Disease-like Type 1 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the PRNP gene associated with Huntington Disease-like 1 (HDL1). HDL1 is a rare neurodegenerative disorder that shares clinical features with Huntington’s disease, including movement disorders, psychiatric symptoms, and cognitive decline, but is caused by different genetic abnormalities. This particular test focuses on identifying the specific mutations in the PRNP gene, which is critical for accurate diagnosis and differentiation from other similar conditions.

Priced at 4400 AED, the test is conducted in the state-of-the-art facilities of DNA Labs UAE, where advanced genetic testing technologies are utilized to ensure high accuracy and reliability of the results. This test is crucial for families with a history of HDL1, as it not only aids in confirming the diagnosis but also helps in understanding the risk of passing the mutation to the next generation. Early and precise diagnosis through the PRNP Gene Huntington Disease-like Type 1 Genetic Test can significantly impact the management and treatment strategies for affected individuals, providing them with a better quality of life.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

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.