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SIGMAR1 Gene Amyotrophic lateral sclerosis type 16 Genetic Test

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

-21%

The SIGMAR1 gene, associated with Amyotrophic Lateral Sclerosis type 16 (ALS16), plays a crucial role in the understanding and diagnosis of this specific form of ALS. Amyotrophic Lateral Sclerosis, also known as Lou Gehrig’s disease, is a progressive neurodegenerative disorder that affects nerve cells in the brain and the spinal cord, leading to muscle weakness and, eventually, severe physical disability.

The genetic test for ALS16 focuses on mutations within the SIGMAR1 gene. Identifying these mutations can be pivotal for families with a history of ALS, as it provides crucial information regarding the inheritance pattern, potential risks to other family members, and contributes to the body of knowledge necessary for future therapeutic developments.

DNA Labs UAE offers this specialized genetic testing service. The test is priced at 4400 AED and is conducted in their state-of-the-art laboratory facilities. By opting for this test at DNA Labs UAE, patients and their families can expect a comprehensive analysis of the SIGMAR1 gene, which will aid in the diagnosis of ALS16. This information can be invaluable for making informed decisions about treatment options and managing the disease more effectively.

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SIGMAR1 Gene Amyotrophic lateral sclerosis type 16 Genetic Test

At DNA Labs UAE, we offer the SIGMAR1 Gene Amyotrophic lateral sclerosis type 16 Genetic Test to help diagnose this rare form of ALS. This test can identify mutations in the SIGMAR1 gene that may cause ALS16.

Test Components and Price

The SIGMAR1 Gene Amyotrophic lateral sclerosis type 16 Genetic Test costs AED 4400.0. The sample condition required for this test is either blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery and Method

After the test is conducted, the report will be delivered within 3 to 4 weeks. The test is performed using NGS (Next Generation Sequencing) technology.

Test Type and Doctor

This genetic test falls under the category of Neurological Disorders. It is recommended to consult a Neurologist for this test.

Test Department and Pre Test Information

This test is conducted in our Genetics department. Before the test, it is important to provide the clinical history of the patient who is going for the SIGMAR1 Gene Amyotrophic lateral sclerosis type 16 NGS Genetic DNA Test. Additionally, a Genetic Counselling session is advised to draw a pedigree chart of family members affected with SIGMAR1 Gene Amyotrophic lateral sclerosis type 16.

Test Details

The SIGMAR1 gene is associated with Amyotrophic lateral sclerosis type 16 (ALS16), which is a rare form of ALS. The NGS Genetic Test involves sequencing the entire SIGMAR1 gene and analyzing the results to identify any mutations that may be present. This information can help doctors diagnose ALS16 and develop appropriate treatment plans for affected individuals.

It is important to note that while genetic testing can be helpful in diagnosing ALS16, it is not a cure for the disease. Treatment options may include medications, physical therapy, and other supportive measures to manage symptoms and improve quality of life.

Test Name SIGMAR1 Gene Amyotrophic lateral sclerosis type 16 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 SIGMAR1 Gene Amyotrophic lateral sclerosis type 16 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SIGMAR1 Gene Amyotrophic lateral sclerosis type 16
Test Details

The SIGMAR1 gene is associated with Amyotrophic lateral sclerosis type 16 (ALS16), a rare form of ALS. NGS (Next Generation Sequencing) Genetic Test is a diagnostic tool that can be used to identify mutations in the SIGMAR1 gene that may cause ALS16. This test involves sequencing the entire SIGMAR1 gene and analyzing the results to identify any mutations that may be present. This information can help doctors diagnose ALS16 and develop appropriate treatment plans for affected individuals. It is important to note that while genetic testing can be helpful in diagnosing ALS16, it is not a cure for the disease. Treatment options may include medications, physical therapy, and other supportive measures to manage symptoms and improve quality of life.