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AIFM1 Gene CMTX4 Genetic Test Cost

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

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The AIFM1 gene CMTX4 genetic test is a specialized diagnostic tool designed to identify mutations in the AIFM1 gene, which are linked to Charcot-Marie-Tooth disease X-linked type 4 (CMTX4). CMTX4 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 limbs. The AIFM1 gene plays a crucial role in maintaining mitochondrial function and its mutations can lead to various neurological symptoms associated with CMTX4.

This genetic test is particularly important for individuals showing symptoms of Charcot-Marie-Tooth disease or those with a family history of the disorder, as it can provide definitive diagnosis and help in the management and treatment planning. It is also valuable for at-risk family members for understanding their risk of developing or passing on the condition.

The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the AIFM1 gene CMTX4 genetic test is 4400 AED. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any mutations in the AIFM1 gene. Results from this test can offer crucial information for genetic counseling and guiding clinical management for affected individuals and their families.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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AIFM1 Gene CMTX4 Genetic Test – DNA Labs UAE

Are you or a loved one experiencing symptoms of Charcot-Marie-Tooth disease type X4 (CMTX4)? DNA Labs UAE offers the AIFM1 Gene CMTX4 Genetic Test to help diagnose this rare inherited neurological disorder. Read on to learn more about the test, its cost, symptoms, diagnosis, and other important details.

Test Name: AIFM1 Gene CMTX4 Genetic Test

Components:

  • Price: 4400.0 AED
  • Sample Condition: Blood
  • 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 AIFM1 Gene CMTX4 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with AIFM1 Gene CMTX4. This information will aid in the accurate interpretation of the test results.

Test Details

The AIFM1 gene is associated with Charcot-Marie-Tooth disease type X4 (CMTX4), a rare inherited neurological disorder that affects the peripheral nerves. The AIFM1 gene is responsible for producing a protein called apoptosis-inducing factor (AIF), which plays a crucial role in cell death and mitochondrial function.

Mutations in the AIFM1 gene can disrupt the normal function of AIF, leading to damage to the nerves that control movement and sensation. To identify these mutations, the AIFM1 Gene CMTX4 Genetic Test utilizes NGS (Next-Generation Sequencing) technology. This advanced sequencing technology analyzes the DNA sequence of the AIFM1 gene and detects any changes or variations that may be present.

NGS genetic testing is highly accurate and can provide a definitive diagnosis of CMTX4. This diagnosis is crucial in guiding appropriate treatment and management strategies for patients with CMTX4. By identifying the specific mutations in the AIFM1 gene, healthcare professionals can develop personalized treatment plans tailored to the individual needs of each patient.

If you or a family member are experiencing symptoms of CMTX4 or have a family history of the condition, it is important to consult with a neurologist. The AIFM1 Gene CMTX4 Genetic Test offered by DNA Labs UAE can provide valuable insights into the diagnosis and management of this rare neurological disorder.

Test Name AIFM1 Gene CMTX4 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
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 AIFM1 Gene CMTX4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with AIFM1 Gene CMTX4
Test Details

The AIFM1 gene is associated with Charcot-Marie-Tooth disease type X4 (CMTX4), a rare inherited neurological disorder that affects the peripheral nerves. The AIFM1 gene provides instructions for making a protein called apoptosis-inducing factor (AIF), which plays a role in cell death and mitochondrial function. Mutations in the AIFM1 gene can disrupt the normal function of AIF, leading to damage to the nerves that control movement and sensation.

NGS genetic testing can identify mutations in the AIFM1 gene that are associated with CMTX4. This type of testing uses advanced sequencing technology to analyze the DNA sequence of the AIFM1 gene and detect any changes or variations that may be present. NGS genetic testing can provide a definitive diagnosis of CMTX4 and help guide appropriate treatment and management strategies.

SKU: TEST-1198 Category:

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