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FLNA Gene FG Syndrome Type 2 Genetic Test

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

-21%

The FLNA gene FG Syndrome Type 2 genetic test is a specialized diagnostic procedure aimed at identifying mutations in the FLNA gene, which are linked to FG Syndrome Type 2, a rare genetic disorder. This condition primarily affects males and can lead to a wide range of physical and developmental challenges, including intellectual disability, skeletal anomalies, and distinctive facial features. The test involves analyzing the patient’s DNA to detect any abnormalities in the FLNA gene that may indicate the presence of the syndrome.

Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers a crucial step towards a definitive diagnosis, enabling healthcare providers to tailor treatment and management plans to the individual needs of the patient. The cost of the FLNA gene FG Syndrome Type 2 genetic test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the FLNA gene. By opting for this test, families and individuals gain valuable insights into their genetic health, paving the way for informed medical decisions and supportive care tailored to those with FG Syndrome Type 2.

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  • This test is not intended for medical diagnosis or treatment
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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.