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9-Sep Gene Amyotrophy hereditary neuralgic Genetic Test

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

-21%

The “9-Sep Gene Amyotrophy Hereditary Neuralgic Genetic Test” is a specialized diagnostic procedure designed to identify genetic mutations associated with hereditary neuralgic amyotrophy (HNA), a rare condition that affects the peripheral nervous system. This condition is characterized by recurrent episodes of nerve pain and muscle weakness, primarily impacting the shoulders and arms. The test focuses on analyzing the 9-Sep gene, which has been closely linked to the development of this condition.

Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers a comprehensive analysis for individuals suspected of having or at risk of developing hereditary neuralgic amyotrophy. By examining the specific genetic markers within the 9-Sep gene, the test can provide valuable insights into the patient’s condition, aiding in the diagnosis and potentially guiding treatment options.

The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic variations associated with HNA. This investment can be invaluable for affected individuals and their families, offering a clearer understanding of the condition and facilitating more informed healthcare decisions.

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  • This test is not intended for medical diagnosis or treatment
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9-Sep Gene Amyotrophy hereditary neuralgic Genetic Test

Components

Price: 4400.0 AED

Sample Condition

Blood

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 9-Sep Gene Amyotrophy hereditary neuralgic NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with 9-Sep Gene Amyotrophy hereditary neuralgic

Test Details

Gene amyotrophy hereditary neuralgic (GAN) is a rare genetic disorder that affects the nervous system and causes muscle weakness and wasting. It is caused by mutations in the SETX gene, which provides instructions for making a protein called senataxin. The senataxin protein is involved in the repair of damaged DNA and the regulation of gene expression.

NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that uses advanced technology to analyze multiple genes at once. This type of testing can be used to identify mutations in the SETX gene that cause GAN.

Hereditary neuralgic amyotrophy (HNA) is a related disorder that is also caused by mutations in the SETX gene. HNA is characterized by recurrent episodes of severe pain and muscle weakness in the shoulders and arms. NGS genetic testing can be used to diagnose both GAN and HNA, as well as to identify carriers of the mutations that cause these disorders. This information can be used to inform reproductive decisions and to provide genetic counseling to affected individuals and their families.

Test Name 9-Sep Gene Amyotrophy hereditary neuralgic Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
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 9-Sep Gene Amyotrophy hereditary neuralgic NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with 9-Sep Gene Amyotrophy hereditary neuralgic
Test Details

Gene amyotrophy hereditary neuralgic (GAN) is a rare genetic disorder that affects the nervous system and causes muscle weakness and wasting. It is caused by mutations in the SETX gene, which provides instructions for making a protein called senataxin. The senataxin protein is involved in the repair of damaged DNA and the regulation of gene expression.

NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that uses advanced technology to analyze multiple genes at once. This type of testing can be used to identify mutations in the SETX gene that cause GAN.

Hereditary neuralgic amyotrophy (HNA) is a related disorder that is also caused by mutations in the SETX gene. HNA is characterized by recurrent episodes of severe pain and muscle weakness in the shoulders and arms.

NGS genetic testing can be used to diagnose both GAN and HNA, as well as to identify carriers of the mutations that cause these disorders. This information can be used to inform reproductive decisions and to provide genetic counseling to affected individuals and their families.

SKU: TEST-1063 Category:

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