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SH3TC2 Gene CMT4C Genetic Test

4,400 د.إ

-21%

The SH3TC2 gene CMT4C genetic test is a specialized diagnostic tool used to detect mutations in the SH3TC2 gene, which are associated with Charcot-Marie-Tooth disease type 4C (CMT4C). CMT4C is a rare form of Charcot-Marie-Tooth disease, a group of disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems primarily in the arms and legs. The test is crucial for confirming the diagnosis, understanding the disease progression, and making informed decisions about management and treatment options.

Performed at DNA Labs UAE, this genetic test involves collecting a DNA sample, usually through a blood draw or a cheek swab, and analyzing the SH3TC2 gene for specific mutations. The accuracy and reliability of the test make it a valuable resource for affected individuals and their families.

The cost of the SH3TC2 gene CMT4C genetic test at DNA Labs UAE is 4400 AED. This investment can provide essential information for the clinical management of patients with or at risk of developing CMT4C, enabling early intervention and personalized care plans to improve quality of life.

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  • 100% accuaret Test Results
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  • This test is not intended for medical diagnosis or treatment
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SH3TC2 Gene CMT4C Genetic Test

Welcome to DNA Labs UAE, where we offer the SH3TC2 Gene CMT4C Genetic Test. This test is designed to diagnose Charcot-Marie-Tooth disease type 4C (CMT4C), a rare genetic disorder affecting the peripheral nerves.

Test Components

The SH3TC2 Gene CMT4C Genetic Test includes the following 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

Before undergoing the SH3TC2 Gene CMT4C NGS Genetic DNA Test, it is important to provide the following:

  • Clinical History of the Patient
  • Genetic Counselling Session to draw a pedigree chart of affected family members

Test Details

The SH3TC2 gene is associated with Charcot-Marie-Tooth disease type 4C (CMT4C). This rare genetic disorder is characterized by muscle weakness and wasting, numbness and tingling in the limbs, and difficulty with balance and coordination.

NGS genetic testing for CMT4C involves sequencing the SH3TC2 gene to identify any mutations or variants that may be causing the disease. This highly accurate and efficient method can be performed using a small blood or saliva sample.

Results from the SH3TC2 Gene CMT4C Genetic Test are typically available within a few weeks. These results can be used to inform treatment decisions and provide genetic counseling for affected individuals and their families.

If you suspect that you or a family member may have CMT4C, we recommend consulting with a neurologist who can guide you through the testing process and provide the necessary support.

Test Name SH3TC2 Gene CMT4C 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 SH3TC2 Gene CMT4C NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SH3TC2 Gene CMT4C
Test Details

The SH3TC2 gene is associated with Charcot-Marie-Tooth disease type 4C (CMT4C), a rare genetic disorder that affects the peripheral nerves. CMT4C is characterized by muscle weakness and wasting, numbness and tingling in the limbs, and difficulty with balance and coordination.

NGS genetic testing for CMT4C involves sequencing the SH3TC2 gene to identify any mutations or variants that may be causing the disease. This type of testing can help diagnose CMT4C and provide information about the severity and progression of the disease.

NGS testing is a highly accurate and efficient method for identifying genetic mutations, and it can be performed using a small blood or saliva sample. Results are typically available within a few weeks, and can be used to inform treatment decisions and provide genetic counseling for affected individuals and their families.