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GDAP1 Gene CMT2K Genetic Test

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

-21%

The GDAP1 Gene CMT2K Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the GDAP1 gene, which are known to cause Charcot-Marie-Tooth disease type 2K (CMT2K), a specific form of Charcot-Marie-Tooth disease. This condition is a hereditary neurological disorder that affects the peripheral nerves, leading to muscle weakness and sensory problems primarily in the limbs.

The test is conducted by collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic alterations in the GDAP1 gene. These mutations disrupt the normal function of the peripheral nerves, resulting in the symptoms associated with CMT2K.

Offered at DNA Labs UAE, the GDAP1 Gene CMT2K Genetic Test is priced at 4400 AED. DNA Labs UAE is a leading facility in the region, equipped with state-of-the-art technology and staffed by genetics professionals to ensure accurate and reliable test results. This test is crucial for individuals with a family history of Charcot-Marie-Tooth disease or those exhibiting symptoms, as it can confirm a diagnosis of CMT2K, inform treatment strategies, and aid in understanding the risk of passing the condition on to future generations.

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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GDAP1 Gene CMT2K Genetic Test

At DNA Labs UAE, we offer the GDAP1 Gene CMT2K Genetic Test for individuals experiencing symptoms related to Charcot-Marie-Tooth (CMT) disease. CMT is a group of inherited neurological disorders that affect the peripheral nerves, leading to muscle weakness, sensory loss, foot deformities, and muscle wasting.

Test Details

The GDAP1 gene is specifically associated with CMT2K, a subtype of CMT disease. To diagnose CMT2K and identify the specific genetic mutation causing the disease, we utilize NGS (next-generation sequencing) technology. NGS allows for the simultaneous analysis of multiple genes, including the GDAP1 gene.

Components and Price

The GDAP1 Gene CMT2K Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or alternatively, one drop of blood on an FTA Card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Test Type and Department

The GDAP1 Gene CMT2K Genetic Test falls under the category of Neurological Disorders and is conducted by our Genetics department.

Pre Test Information

Before undergoing the GDAP1 Gene CMT2K NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to create a pedigree chart of family members affected by GDAP1 Gene CMT2K.

Benefits of NGS Genetic Testing

NGS genetic testing not only aids in the diagnosis of CMT2K but also provides valuable information about the specific genetic mutation causing the disease. This information can be used to guide treatment and management strategies. Furthermore, it offers important insights for family members who may also be at risk for the condition.

Consultation with a Neurologist

Our experienced Neurologist will be available to discuss the test results and provide further guidance based on the diagnosis.

Don’t let the symptoms of CMT2K go undiagnosed. Contact DNA Labs UAE today to schedule the GDAP1 Gene CMT2K Genetic Test and take control of your health.

Test Name GDAP1 Gene CMT2K 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 GDAP1 Gene CMT2K NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GDAP1 Gene CMT2K
Test Details

The GDAP1 gene is associated with a type of Charcot-Marie-Tooth (CMT) disease called CMT2K. CMT is a group of inherited neurological disorders that affect the peripheral nerves, causing muscle weakness and wasting, sensory loss, and foot deformities.

NGS (next-generation sequencing) genetic testing is a method of analyzing DNA that allows for the simultaneous analysis of multiple genes. This type of testing can be used to identify mutations in the GDAP1 gene that are associated with CMT2K.

NGS genetic testing can be helpful in diagnosing CMT2K and providing information about the specific genetic mutation that is causing the disease. This information can be used to guide treatment and management strategies and provide important information for family members who may also be at risk for the condition.