FLNA Gene FG Syndrome Type 2 Genetic Test
Test Components:
- FLNA Gene FG Syndrome 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
Test Type:
Neurological Disorders
Doctor:
Neurologist
Test Department:
Genetics
Pre Test Information:
Clinical History of Patient who is going for FLNA Gene FG Syndrome Type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FLNA Gene FG Syndrome Type 2.
Test Details:
FLNA gene FG Syndrome Type 2 NGS genetic test is a type of genetic testing that is used to identify mutations in the FLNA gene that cause FG Syndrome Type 2. FG Syndrome is a rare genetic disorder that affects the development of the nervous system and causes intellectual disability, facial abnormalities, and other physical and behavioral problems. The FLNA gene provides instructions for making a protein called filamin A, which is important for the development and maintenance of the cytoskeleton, the network of protein fibers that gives cells their shape and helps them maintain their structure. Mutations in the FLNA gene can disrupt the normal function of filamin A, leading to the symptoms of FG Syndrome. NGS (next-generation sequencing) is a high-throughput method of DNA sequencing that allows for the rapid and efficient analysis of large amounts of genetic information. NGS technology is used to sequence the FLNA gene and identify any mutations that may be present. The FLNA gene FG Syndrome Type 2 NGS genetic test can be used to confirm a diagnosis of FG Syndrome Type 2 in individuals with symptoms of the condition. It can also be used to identify carriers of the mutated gene in families with a history of the disorder. Genetic counseling may be recommended for individuals who test positive for mutations in the FLNA gene.
Test Name | FLNA Gene FG syndrome 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 FLNA Gene FG syndrome type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FLNA Gene FG syndrome type 2 |
Test Details | FLNA gene FG syndrome type 2 NGS genetic test is a type of genetic testing that is used to identify mutations in the FLNA gene that cause FG syndrome type 2. FG syndrome is a rare genetic disorder that affects the development of the nervous system and causes intellectual disability, facial abnormalities, and other physical and behavioral problems. The FLNA gene provides instructions for making a protein called filamin A, which is important for the development and maintenance of the cytoskeleton, the network of protein fibers that gives cells their shape and helps them maintain their structure. Mutations in the FLNA gene can disrupt the normal function of filamin A, leading to the symptoms of FG syndrome. NGS (next-generation sequencing) is a high-throughput method of DNA sequencing that allows for the rapid and efficient analysis of large amounts of genetic information. NGS technology is used to sequence the FLNA gene and identify any mutations that may be present. The FLNA gene FG syndrome type 2 NGS genetic test can be used to confirm a diagnosis of FG syndrome type 2 in individuals with symptoms of the condition. It can also be used to identify carriers of the mutated gene in families with a history of the disorder. Genetic counseling may be recommended for individuals who test positive for mutations in the FLNA gene. |