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FIG4 Gene CMT4J Genetic Test

4,400 د.إ

-21%

The FIG4 Gene CMT4J Genetic Test is a specialized diagnostic tool designed to detect mutations in the FIG4 gene, which are linked to Charcot-Marie-Tooth disease type 4J (CMT4J). CMT4J is a rare and severe neurological disorder characterized by progressive weakness and atrophy of the muscles in the feet, hands, and elsewhere. The condition can also affect sensory nerves, leading to a loss of sensation in the affected areas.

This genetic test is crucial for individuals suspected of having CMT4J based on clinical symptoms or family history. Early and accurate diagnosis through the FIG4 Gene CMT4J Genetic Test allows for better management of the condition, including therapeutic interventions and genetic counseling for affected families.

The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED. DNA Labs UAE utilizes state-of-the-art technology and adheres to the highest standards of accuracy and reliability in genetic diagnostics, ensuring that individuals receive comprehensive and precise information about their genetic health.

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FIG4 Gene CMT4J Genetic Test

Test Name: FIG4 Gene CMT4J Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 FIG4 Gene CMT4J NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FIG4 Gene CMT4J.

Test Details: The FIG4 gene is associated with a rare form of Charcot-Marie-Tooth (CMT) disease called CMT4J. CMT is a group of inherited disorders that affect the peripheral nerves, which control muscle movement and sensation. CMT4J is caused by mutations in the FIG4 gene, which provides instructions for making a protein that helps to regulate the flow of materials in and out of cells. NGS (next-generation sequencing) genetic testing is a type of DNA testing that can detect mutations in the FIG4 gene associated with CMT4J. This test involves sequencing the entire coding region of the FIG4 gene, which includes all the exons and introns. NGS technology allows for the rapid and accurate detection of mutations in multiple genes at once, making it a useful tool for diagnosing rare genetic disorders like CMT4J. NGS genetic testing for CMT4J can be done using a blood or saliva sample. The sample is sent to a laboratory that specializes in genetic testing, where the DNA is extracted and sequenced using NGS technology. The results of the test can help to confirm a diagnosis of CMT4J, which can be important for guiding treatment and management strategies for affected individuals and their families.

Test Name FIG4 Gene CMT4J 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 FIG4 Gene CMT4J NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FIG4 Gene CMT4J
Test Details

The FIG4 gene is associated with a rare form of Charcot-Marie-Tooth (CMT) disease called CMT4J. CMT is a group of inherited disorders that affect the peripheral nerves, which control muscle movement and sensation. CMT4J is caused by mutations in the FIG4 gene, which provides instructions for making a protein that helps to regulate the flow of materials in and out of cells.

NGS (next-generation sequencing) genetic testing is a type of DNA testing that can detect mutations in the FIG4 gene associated with CMT4J. This test involves sequencing the entire coding region of the FIG4 gene, which includes all the exons and introns. NGS technology allows for the rapid and accurate detection of mutations in multiple genes at once, making it a useful tool for diagnosing rare genetic disorders like CMT4J.

NGS genetic testing for CMT4J can be done using a blood or saliva sample. The sample is sent to a laboratory that specializes in genetic testing, where the DNA is extracted and sequenced using NGS technology. The results of the test can help to confirm a diagnosis of CMT4J, which can be important for guiding treatment and management strategies for affected individuals and their families.