SCN4A Gene Myasthenic Syndrome Due to Mutation in SCN4A Genetic Test sale cost 4400 AED
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SCN4A Gene Myasthenic Syndrome Due to Mutation in SCN4A Genetic Test Cost

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

-21%

The SCN4A gene myasthenic syndrome is a rare genetic condition characterized by muscle weakness and fatigue. This condition is caused by mutations in the SCN4A gene, which plays a crucial role in the normal functioning of muscle cells. The SCN4A gene encodes a component of sodium channels that are essential for the transmission of electrical signals in muscle cells, facilitating muscle contraction. Mutations in this gene can disrupt the normal flow of sodium ions, leading to the symptoms associated with the syndrome.

To diagnose this condition, a specific genetic test is available that identifies mutations in the SCN4A gene. This test is crucial for confirming the diagnosis, understanding the severity of the condition, and guiding treatment decisions. The test involves collecting a DNA sample, usually through a blood draw, and analyzing the genetic material for mutations in the SCN4A gene.

In the United Arab Emirates, this genetic test is offered by DNA Labs UAE, a reputable facility known for its advanced diagnostic services. The cost of the SCN4A gene myasthenic syndrome genetic test at DNA Labs UAE is 4400 AED. This test is a valuable tool for individuals experiencing symptoms of muscle weakness and fatigue, providing them with a definitive diagnosis and enabling them to seek appropriate treatment and management strategies for their condition.

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SCN4A Gene Myasthenic Syndrome: Symptoms, Diagnosis, and Genetic Test Cost

SCN4A gene myasthenic syndrome is a rare genetic disorder caused by mutations in the SCN4A gene. This gene provides instructions for making a protein called the sodium channel alpha subunit 4 (Nav1.4), which is involved in the transmission of electrical signals in muscle cells. Mutations in the SCN4A gene can disrupt the normal functioning of Nav1.4 channels, leading to impaired muscle contraction and weakness.

This condition is characterized by muscle weakness and fatigue that worsens with exertion, as well as other symptoms such as muscle cramps, stiffness, and myotonia (delayed muscle relaxation).

To diagnose SCN4A gene myasthenic syndrome, a genetic test is required. The SCN4A Gene Myasthenic Syndrome Genetic Test offered by DNA Labs UAE is a comprehensive test that analyzes the SCN4A gene for mutations. The test utilizes Next-Generation Sequencing (NGS) technology, which allows for the simultaneous sequencing of multiple genes, making it an efficient and cost-effective method for genetic testing.

Test Details

  • Test Name: SCN4A Gene Myasthenic Syndrome due to mutation in SCN4A Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the SCN4A Gene Myasthenic Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by SCN4A Gene Myasthenic Syndrome.

Diagnosis and Management

Genetic testing plays a crucial role in accurately diagnosing SCN4A gene myasthenic syndrome. By identifying mutations in the SCN4A gene, healthcare professionals can confirm the diagnosis and provide valuable information for genetic counseling. Although there is currently no cure for SCN4A gene myasthenic syndrome, management options focus on symptom relief and improving the patient’s quality of life.

For individuals interested in undergoing the SCN4A Gene Myasthenic Syndrome Genetic Test, DNA Labs UAE offers the test at a cost of 4400.0 AED. The test can be conducted using a blood sample or extracted DNA, or by collecting one drop of blood on an FTA card. The report delivery time is estimated to be 3 to 4 weeks.

By utilizing NGS technology, DNA Labs UAE ensures accurate and efficient genetic testing for neurological disorders such as SCN4A gene myasthenic syndrome. The test is conducted by experienced neurologists in the genetics department, guaranteeing reliable results.

Genetic testing not only aids in diagnosis but also helps guide treatment decisions and provides valuable information for genetic counseling. By understanding the genetic basis of SCN4A gene myasthenic syndrome, healthcare professionals can develop personalized treatment plans and offer support to affected individuals and their families.

Test Name SCN4A Gene Myasthenic syndrome due to mutation in SCN4A 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 SCN4A Gene Myasthenic syndrome due to mutation in SCN4A NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SCN4A Gene Myasthenic syndrome due to mutation in SCN4A
Test Details

SCN4A gene myasthenic syndrome is a rare genetic disorder caused by mutations in the SCN4A gene. This gene provides instructions for making a protein called the sodium channel alpha subunit 4 (Nav1.4), which is involved in the transmission of electrical signals in muscle cells.

Mutations in the SCN4A gene can disrupt the normal functioning of Nav1.4 channels, leading to impaired muscle contraction and weakness. This condition is characterized by muscle weakness and fatigue that worsens with exertion, as well as other symptoms such as muscle cramps, stiffness, and myotonia (delayed muscle relaxation).

NGS (Next-Generation Sequencing) genetic testing is a powerful tool used to identify mutations in the SCN4A gene and diagnose SCN4A gene myasthenic syndrome. NGS allows for the simultaneous sequencing of multiple genes, making it an efficient and cost-effective method for genetic testing.

During NGS testing, DNA samples from the patient are sequenced, and the resulting data is analyzed to identify any genetic variants or mutations in the SCN4A gene. These mutations can then be correlated with the symptoms and clinical presentation to confirm a diagnosis of SCN4A gene myasthenic syndrome.

Genetic testing is important for accurate diagnosis, as it can help guide treatment decisions and provide valuable information for genetic counseling. While there is currently no cure for SCN4A gene myasthenic syndrome, management options focus on symptom relief and improving quality of life.

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