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HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive Genetic Test Cost

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

-21%

The “HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive Genetic Test” is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the HINT1 gene. This gene is crucial because mutations within it are linked to the development of neuromyotonia and axonal neuropathy, conditions that affect the nervous system leading to muscle stiffness and weakness, among other symptoms. These disorders are inherited in an autosomal recessive pattern, meaning an individual must receive a mutated gene from both parents to be affected.

The test, which costs 4400 AED, is a vital tool for families with a history of these conditions, providing them with crucial information regarding their genetic status. Early detection through this genetic testing can facilitate timely intervention and management of the conditions, potentially improving the quality of life for those affected. DNA Labs UAE utilizes advanced genetic testing technologies to ensure accurate and reliable results, making it a trusted choice for individuals seeking clarity about their genetic health concerning the HINT1 gene.

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  • This test is not intended for medical diagnosis or treatment
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HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive Genetic Test

At DNA Labs UAE, we offer the HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive Genetic Test. This test helps in diagnosing a rare genetic disorder characterized by muscle stiffness, cramps, and twitching (neuromyotonia) as well as nerve damage (axonal neuropathy). The disorder is inherited in an autosomal recessive manner, meaning that both copies of the HINT1 gene must be mutated for the disorder to manifest.

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

Before undergoing the HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive 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 HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive.

Test Details

The HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive Genetic Test involves a Next-Generation Sequencing (NGS) technology. This powerful technology allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. To perform the test, DNA is extracted from a patient’s blood or saliva sample. The DNA is then sequenced, and the data is analyzed to identify any mutations or variations in the HINT1 gene.

If two pathogenic mutations are found in the HINT1 gene, it confirms the diagnosis of HINT1 Gene Neuromyotonia. Genetic testing plays a crucial role in confirming the diagnosis, providing information about disease progression, and guiding treatment options. It is highly recommended to consult with a genetic counselor or healthcare professional for a comprehensive evaluation and interpretation of the genetic test results.

For more information or to schedule an appointment, please contact DNA Labs UAE.

Test Name HINT1 Gene Neuromyotonia and axonal neuropathy autosomal recessive 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 HINT1 Gene Neuromyotonia and axonal neuropathy, autosomal recessive NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HINT1 Gene Neuromyotonia and axonal neuropathy, autosomal recessive
Test Details

HINT1 Gene Neuromyotonia is a rare genetic disorder characterized by muscle stiffness, cramps, and twitching (neuromyotonia) as well as nerve damage (axonal neuropathy). It is inherited in an autosomal recessive manner, meaning that both copies of the HINT1 gene must be mutated for the disorder to manifest.

To diagnose HINT1 Gene Neuromyotonia, a Next-Generation Sequencing (NGS) genetic test can be performed. NGS is a powerful technology that allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup.

The NGS genetic test for HINT1 Gene Neuromyotonia involves extracting DNA from a patient’s blood or saliva sample. The DNA is then sequenced, and the data is analyzed to identify any mutations or variations in the HINT1 gene. If two pathogenic mutations are found in the HINT1 gene, it confirms the diagnosis of HINT1 Gene Neuromyotonia.

Genetic testing can help in confirming the diagnosis, providing information about disease progression, and guiding treatment options. It is essential to consult with a genetic counselor or healthcare professional for a comprehensive evaluation and interpretation of the genetic test results.

SKU: TEST-1849 Category:

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