NDRG1 Gene CMT4D Genetic Test
At DNA Labs UAE, we offer the NDRG1 Gene CMT4D Genetic Test for individuals who are experiencing symptoms related to Charcot-Marie-Tooth disease type 4D (CMT4D). This rare inherited disorder affects the peripheral nerves and can cause a range of neurological symptoms.
Test Details
The NDRG1 gene is associated with CMT4D, and our NGS (next-generation sequencing) technology allows us to analyze the DNA sequence of this gene. By identifying any mutations or changes in the NDRG1 gene, we can help diagnose CMT4D in patients who are showing symptoms of the disorder.
The NDRG1 Gene CMT4D Genetic Test involves taking a small sample of the patient’s DNA, which can be obtained from blood or extracted DNA. Alternatively, a single drop of blood can be collected on an FTA card. This sample is then analyzed using NGS technology, which is a highly sensitive and accurate method of identifying genetic mutations.
Once the sample is received, our team will deliver the test report within 3 to 4 weeks. This report will provide detailed information about the patient’s NDRG1 gene and any abnormalities that may have been identified.
Cost and Test Department
The NDRG1 Gene CMT4D Genetic Test is priced at 4400.0 AED. This test falls under our Genetics department, as it focuses on the genetic factors associated with neurological disorders.
Pre Test Information
Prior to undergoing the NDRG1 Gene CMT4D Genetic Test, it is important for the patient to provide their clinical history. This information helps our team understand the patient’s symptoms and medical background, which can aid in the interpretation of the test results.
In addition, a genetic counseling session may be conducted to draw a pedigree chart of family members who have been affected by NDRG1 Gene CMT4D. This can provide valuable insights into the inheritance pattern of the disorder within the family.
Importance of NDRG1 Gene CMT4D Genetic Test
Diagnosing CMT4D through the NDRG1 Gene CMT4D Genetic Test can be crucial for guiding treatment decisions and providing important information for genetic counseling and family planning. Identifying a mutation in the NDRG1 gene can help healthcare providers tailor treatment plans to the specific needs of the patient.
Furthermore, NGS genetic testing is becoming increasingly accessible and affordable for patients. It is a powerful tool for diagnosing genetic disorders like CMT4D, but it is important to work with a qualified healthcare provider who can interpret the test results and provide appropriate treatment and support.
At DNA Labs UAE, we have a team of experienced neurologists who specialize in the diagnosis and management of neurological disorders. Our goal is to provide accurate and timely genetic testing services to individuals who may be affected by CMT4D or other related conditions.
Contact us today to learn more about the NDRG1 Gene CMT4D Genetic Test and how it can help in diagnosing and managing this rare inherited disorder.
Test Name | NDRG1 Gene CMT4D 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 NDRG1 Gene CMT4D NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDRG1 Gene CMT4D |
Test Details |
The NDRG1 gene is associated with Charcot-Marie-Tooth disease type 4D (CMT4D), which is a rare inherited disorder that affects the peripheral nerves. NGS (next-generation sequencing) genetic testing is a method of analyzing the DNA sequence of the NDRG1 gene to identify any mutations or changes that may be causing CMT4D. NGS genetic testing is a highly sensitive and accurate method of identifying genetic mutations, and it can help diagnose CMT4D in patients who are showing symptoms of the disorder. The test involves taking a small sample of the patient’s DNA and sequencing the NDRG1 gene to look for any abnormalities. If a mutation is identified in the NDRG1 gene, the patient may be diagnosed with CMT4D. This can help guide treatment decisions and provide important information for genetic counseling and family planning. NGS genetic testing is a powerful tool for diagnosing genetic disorders like CMT4D, and it is becoming increasingly accessible and affordable for patients. However, it is important to work with a qualified healthcare provider who can interpret the results of the test and provide appropriate treatment and support. |