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FGD4 Gene CMT4H Genetic Test

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

-21%

The FGD4 gene CMT4H genetic test is a specialized diagnostic tool used to detect mutations in the FGD4 gene, which are responsible for causing Charcot-Marie-Tooth disease type 4H (CMT4H). CMT4H is a rare form of Charcot-Marie-Tooth disease, a neurological disorder that leads to peripheral nerve damage. This condition typically manifests in early childhood and is characterized by muscle weakness, sensory loss, and potential deformities in the feet and hands.

The test is crucial for individuals showing symptoms of CMT4H or those with a family history of the condition, as it provides definitive genetic evidence of the disorder. Early diagnosis through genetic testing can aid in the management of symptoms and improve the quality of life for affected individuals.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The cost of the FGD4 gene CMT4H genetic test is 4400 AED. The test is conducted under stringent laboratory conditions by highly qualified professionals, ensuring that patients receive precise results for effective disease management and counseling.

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  • This test is not intended for medical diagnosis or treatment
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FGD4 Gene CMT4H Genetic Test

Welcome to DNA Labs UAE, a leading genetic laboratory specializing in DNA testing. In this blog post, we will discuss the FGD4 Gene CMT4H Genetic Test, its components, cost, symptoms, diagnosis process, and more.

Test Details

The FGD4 gene is associated with a type of Charcot-Marie-Tooth (CMT) disease called CMT4H. CMT is a group of inherited disorders that affect the peripheral nerves, which control movement and sensation in the limbs. CMT4H is a rare subtype of CMT that is caused by mutations in the FGD4 gene.

NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced technology to rapidly sequence large amounts of DNA. NGS testing can be used to identify mutations in the FGD4 gene that cause CMT4H. This type of testing is particularly useful for identifying genetic mutations in rare diseases like CMT4H, which may be missed by traditional genetic testing methods.

Test Name

FGD4 Gene CMT4H Genetic Test

Components

  • 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

Prior to undergoing the FGD4 Gene CMT4H NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with FGD4 Gene CMT4H.

Diagnosis and Symptoms

The FGD4 Gene CMT4H Genetic Test helps in diagnosing CMT4H and provides information about the patient’s risk of passing the condition on to their children. Common symptoms of CMT4H include peripheral neuropathy, muscle weakness, foot deformities, and impaired sensation in the limbs.

If you suspect that you or a family member may have CMT4H, it is recommended to consult with a neurologist who specializes in neurological disorders.

Conclusion

The FGD4 Gene CMT4H Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing and understanding CMT4H. With the use of NGS technology, this test can accurately identify mutations in the FGD4 gene that cause CMT4H. Early diagnosis and genetic counseling can help patients and their families make informed decisions about their health and future.

For more information or to schedule a consultation, please contact DNA Labs UAE.

Test Name FGD4 Gene CMT4H 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 FGD4 Gene CMT4H NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FGD4 Gene CMT4H
Test Details

The FGD4 gene is associated with a type of Charcot-Marie-Tooth (CMT) disease called CMT4H. CMT is a group of inherited disorders that affect the peripheral nerves, which control movement and sensation in the limbs. CMT4H is a rare subtype of CMT that is caused by mutations in the FGD4 gene.

NGS (next-generation sequencing) genetic testing is a type of genetic testing that uses advanced technology to rapidly sequence large amounts of DNA. NGS testing can be used to identify mutations in the FGD4 gene that cause CMT4H. This type of testing is particularly useful for identifying genetic mutations in rare diseases like CMT4H, which may be missed by traditional genetic testing methods.

NGS testing for CMT4H typically involves collecting a blood or saliva sample from the patient and analyzing their DNA for mutations in the FGD4 gene. The results of the test can help diagnose CMT4H and provide information about the patient’s risk of passing the condition on to their children. Genetic counseling is often recommended for patients and their families following a positive test result.