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CASK Gene FG Syndrome Type 4 Genetic Test

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

-21%

The CASK Gene FG Syndrome Type 4 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the CASK gene, which are associated with FG Syndrome Type 4. This condition is a rare genetic disorder that affects various parts of the body, including the nervous system, leading to developmental delays, intellectual disability, and physical anomalies. The test is crucial for early detection and management of the syndrome, ensuring that individuals receive the appropriate care and interventions. Priced at 4400 AED, this test is a vital resource for families and healthcare providers seeking to understand the genetic underpinnings of FG Syndrome Type 4, facilitating personalized treatment plans and support for affected individuals.

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CASK Gene FG Syndrome Type 4 Genetic Test

Test Name: CASK Gene FG Syndrome Type 4 Genetic Test

Components: CASK 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 CASK Gene FG Syndrome Type 4 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CASK Gene FG Syndrome Type 4.

Test Details:

The CASK Gene FG Syndrome Type 4 NGS genetic test is a diagnostic test that analyzes the CASK gene for mutations associated with FG syndrome type 4. FG syndrome is a rare genetic disorder that affects multiple systems in the body, including the nervous system, causing intellectual disability, developmental delays, and physical abnormalities.

FG syndrome type 4 is caused by mutations in the CASK gene, which provides instructions for making a protein that is important for the development and function of the nervous system.

NGS, or next-generation sequencing, is a powerful genetic testing technology that can analyze multiple genes simultaneously, allowing for faster and more comprehensive testing. The CASK gene FG syndrome type 4 NGS genetic test involves taking a sample of the patient’s DNA, usually through a blood sample, and analyzing it for mutations in the CASK gene using NGS technology.

If a mutation is found in the CASK gene, it confirms a diagnosis of FG syndrome type 4 and can help guide treatment and management of the disorder. Genetic testing can also provide valuable information for family planning and genetic counseling.

Test Name CASK Gene FG syndrome type 4 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 CASK Gene FG syndrome type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CASK Gene FG syndrome type 4
Test Details

The CASK gene FG syndrome type 4 NGS genetic test is a diagnostic test that analyzes the CASK gene for mutations associated with FG syndrome type 4. FG syndrome is a rare genetic disorder that affects multiple systems in the body, including the nervous system, causing intellectual disability, developmental delays, and physical abnormalities. FG syndrome type 4 is caused by mutations in the CASK gene, which provides instructions for making a protein that is important for the development and function of the nervous system.

NGS, or next-generation sequencing, is a powerful genetic testing technology that can analyze multiple genes simultaneously, allowing for faster and more comprehensive testing. The CASK gene FG syndrome type 4 NGS genetic test involves taking a sample of the patient’s DNA, usually through a blood sample, and analyzing it for mutations in the CASK gene using NGS technology.

If a mutation is found in the CASK gene, it confirms a diagnosis of FG syndrome type 4 and can help guide treatment and management of the disorder. Genetic testing can also provide valuable information for family planning and genetic counseling.