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GJC2 Gene SPG44 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The GJC2 Gene SPG44 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the GJC2 gene, which are associated with Spastic Paraplegia 44 (SPG44), a rare form of hereditary spastic paraplegia. This condition is characterized by progressive weakness and spasticity, primarily in the lower limbs, and can lead to severe mobility issues. The test involves analyzing the patient’s DNA to detect specific genetic alterations in the GJC2 gene that are known to cause SPG44.

Performed at DNA Labs UAE, a leading facility in genetic testing, this test is crucial for individuals with a family history of hereditary spastic paraplegia or those exhibiting symptoms, providing them with a definitive diagnosis. Early detection through this genetic test can significantly aid in managing the condition, allowing for appropriate therapeutic interventions and genetic counseling for affected families.

The cost of the GJC2 Gene SPG44 Genetic Test at DNA Labs UAE is 4400 AED, reflecting the comprehensive analysis and detailed insights it provides into the patient’s genetic makeup regarding SPG44. This investment in health can be invaluable for affected individuals and their families, offering clarity on the condition and guidance on how to best manage it.

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
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GJC2 Gene SPG44 Genetic Test

At DNA Labs UAE, we offer the GJC2 Gene SPG44 Genetic Test for individuals suspected to have hereditary spastic paraplegia (SPG44). This rare genetic disorder is characterized by progressive stiffness and weakness of the legs due to nerve fiber degeneration.

Test Details

The GJC2 gene, also known as the gap junction protein gamma-2 gene, is associated with SPG44. Our Next-Generation Sequencing (NGS) technology allows us to analyze multiple genes simultaneously, including the GJC2 gene and other relevant genes associated with SPG44. This comprehensive approach enables us to detect genetic variations and confirm a diagnosis of SPG44.

Test Components and Price

The GJC2 Gene SPG44 Genetic Test costs AED 4400.0. The sample condition required for testing can be either blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

After sample collection, the report will be delivered within 3 to 4 weeks. Our NGS technology ensures accurate and efficient analysis of the genetic material.

Test Type and Doctor

The GJC2 Gene SPG44 Genetic Test falls under the category of Neurological Disorders. It is recommended to consult a neurologist for this specific test.

Test Department and Pre-Test Information

The GJC2 Gene SPG44 Genetic Test is conducted in our Genetics department. Prior to the test, it is essential 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 SPG44.

Importance of Genetic Testing for SPG44

Genetic testing for SPG44 can confirm a diagnosis and provide crucial information for genetic counseling and management of the condition. It is highly recommended to seek the expertise of a qualified healthcare professional or genetic counselor to interpret the test results and receive appropriate guidance and support.

Test Name GJC2 Gene SPG44 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 GJC2 Gene SPG44 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GJC2 Gene SPG44
Test Details

The GJC2 gene, also known as the gap junction protein gamma-2 gene, is associated with a specific form of hereditary spastic paraplegia called SPG44. SPG44 is a rare genetic disorder characterized by progressive stiffness and weakness of the legs (paraplegia) due to degeneration of the nerve fibers that control muscle movement.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of genetic variations, such as mutations or changes, in the GJC2 gene and other relevant genes associated with SPG44. This test can help confirm a diagnosis of SPG44 and provide important information for genetic counseling and management of the condition.

It is important to note that genetic testing for SPG44 should be performed by a qualified healthcare professional or a genetic counselor who can interpret the results and provide appropriate guidance and support.

SKU: TEST-2009 Category:

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