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JPH3 Gene Huntington Disease-like Type 2 Genetic Test

4,400 د.إ

-21%

The JPH3 gene Huntington Disease-like Type 2 genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the JPH3 gene, which are associated with Huntington Disease-like 2 (HDL2). HDL2 is a rare neurodegenerative disorder that shares many clinical features with Huntington’s disease, including movement disorders, psychiatric disturbances, and cognitive decline. The condition is inherited in an autosomal dominant pattern, meaning a mutation in just one of the two copies of the JPH3 gene can lead to the disease.

This test is crucial for individuals with a family history of HDL2 or those exhibiting symptoms suggestive of Huntington’s disease but who have tested negative for the more common HTT gene mutation associated with Huntington’s. Early and accurate diagnosis through the JPH3 gene test can facilitate better management of the condition, allow for genetic counseling, and inform family planning decisions.

The test is conducted at DNA Labs UAE, a facility renowned for its state-of-the-art genetic testing services. The cost of the test is set at 4400 AED, reflecting the specialized nature of the analysis and the expertise required to interpret the results accurately. By opting for this test, patients and their families can gain valuable insights into their genetic status and take proactive steps in managing their health.

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JPH3 Gene Huntington disease-like type 2 Genetic Test

Introduction

The JPH3 Gene Huntington disease-like type 2 Genetic Test is a specialized neurogenetic test offered by DNA Labs UAE. This test is designed to identify mutations or variations in the JPH3 gene that may be associated with Huntington disease-like type 2 (HDL2), a rare neurodegenerative disorder.

Test Components

  • Test Name: JPH3 Gene Huntington disease-like 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 (Next-Generation Sequencing)
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics
  • Pre Test Information: Clinical History of Patient who is going for JPH3 Gene Huntington disease-like type 2 NGS Genetic DNA Test, Genetic Counselling session to draw a pedigree chart of family members affected with JPH3 Gene Huntington disease-like type 2

Understanding HDL2

Huntington disease-like type 2 (HDL2) is a rare neurodegenerative disorder that shares some similarities with Huntington’s disease. It is characterized by movement problems, psychiatric symptoms, and cognitive decline. The JPH3 gene is associated with HDL2.

NGS Genetic Testing for HDL2

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. In the case of HDL2, NGS can be used to identify mutations or variations in the JPH3 gene that may be associated with the disease. This involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the JPH3 gene to look for any abnormalities.

Importance of Professional Interpretation

It’s important to note that genetic testing for HDL2 should be done in specialized genetic testing laboratories and ordered and interpreted by healthcare professionals with expertise in genetic testing and neurogenetics. The results of the genetic test can help guide treatment and management options for individuals with HDL2.

Conclusion

The JPH3 Gene Huntington disease-like type 2 Genetic Test offered by DNA Labs UAE is a valuable tool in diagnosing HDL2. With its NGS technology, this test can identify mutations or variations in the JPH3 gene and provide important information for treatment and management. If you suspect HDL2 in yourself or a family member, consult with a neurologist and consider undergoing this genetic test.

Test Name JPH3 Gene Huntington disease-like type 2 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 JPH3 Gene Huntington disease-like type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with JPH3 Gene Huntington disease-like type 2
Test Details

The JPH3 gene is associated with Huntington disease-like type 2 (HDL2), which is a rare neurodegenerative disorder that shares some similarities with Huntington’s disease. HDL2 is characterized by movement problems, psychiatric symptoms, and cognitive decline.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. In the case of HDL2, NGS can be used to identify mutations or variations in the JPH3 gene that may be associated with the disease.

NGS genetic testing for HDL2 involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the JPH3 gene to look for any abnormalities. This can help confirm a diagnosis of HDL2 and provide information about the specific genetic variant involved.

It’s important to note that genetic testing for HDL2 is typically done in specialized genetic testing laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetic testing and neurogenetics. The results of the genetic test can help guide treatment and management options for individuals with HDL2.