PFN1 Gene Amyotrophic Lateral Sclerosis Type 18 Genetic Test
Test Name: PFN1 Gene Amyotrophic Lateral Sclerosis Type 18 Genetic Test
Components: PFN1 Gene Analysis
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 PFN1 Gene Amyotrophic Lateral Sclerosis Type 18 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PFN1 Gene Amyotrophic Lateral Sclerosis Type 18.
Test Details
The PFN1 gene is associated with Amyotrophic Lateral Sclerosis Type 18 (ALS18), a rare form of ALS that is inherited in an autosomal dominant manner. NGS (next-generation sequencing) genetic testing can be used to analyze the PFN1 gene for mutations that may cause ALS18. This type of testing can help diagnose ALS18 in individuals who have symptoms of the disease and a family history of ALS. It can also be used for genetic counseling and to identify carriers of the mutation in families with a history of ALS18. However, it is important to note that not all cases of ALS18 are caused by mutations in the PFN1 gene, and other genes may also be involved.
Test Name | PFN1 Gene Amyotrophic lateral sclerosis type 18 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 PFN1 Gene Amyotrophic lateral sclerosis type 18 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PFN1 Gene Amyotrophic lateral sclerosis type 18 |
Test Details |
The PFN1 gene is associated with Amyotrophic lateral sclerosis type 18 (ALS18), a rare form of ALS that is inherited in an autosomal dominant manner. NGS (next-generation sequencing) genetic testing can be used to analyze the PFN1 gene for mutations that may cause ALS18. This type of testing can help diagnose ALS18 in individuals who have symptoms of the disease and a family history of ALS. It can also be used for genetic counseling and to identify carriers of the mutation in families with a history of ALS18. However, it is important to note that not all cases of ALS18 are caused by mutations in the PFN1 gene, and other genes may also be involved. |