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SCN4A Gene Potassium-Aggravated Myotonia Genetic Test Cost

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

-21%

The SCN4A gene potassium-aggravated myotonia genetic test is a specialized diagnostic procedure designed to identify mutations in the SCN4A gene, which are known to cause potassium-aggravated myotonia. This condition is a type of myotonia, characterized by muscle stiffness that worsens with potassium-rich foods or activities that increase potassium levels in the blood. The SCN4A gene plays a crucial role in the function of sodium channels in muscle cells, and mutations can disrupt normal muscle relaxation, leading to symptoms of stiffness and muscle weakness.

Conducted at DNA Labs UAE, this test offers a precise method for diagnosing individuals who may exhibit symptoms of potassium-aggravated myotonia, enabling healthcare providers to tailor treatment plans more effectively. The test is priced at 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to interpret the results. Through a simple blood sample, the test searches for specific genetic alterations in the SCN4A gene, providing insights that are critical for understanding the condition and exploring potential therapeutic strategies. This test represents an important tool in the field of genetic diagnostics, offering hope and direction for individuals affected by this rare muscular disorder.

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SCN4A Gene Potassium-aggravated myotonia Genetic Test

Cost: 4400.0 AED

Test Components:

  • 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:

Clinical History of Patient who is going for SCN4A Gene Potassium-aggravated myotonia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN4A Gene Potassium-aggravated myotonia.

Test Details:

The SCN4A gene is responsible for encoding a protein called the sodium channel voltage-gated type IV alpha subunit. Mutations in this gene can lead to a condition called potassium-aggravated myotonia. Potassium-aggravated myotonia is a type of muscle disorder characterized by muscle stiffness and delayed relaxation after contraction. This condition is worsened by high levels of potassium in the blood, which can be triggered by factors such as exercise, stress, or certain medications.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes. In the case of potassium-aggravated myotonia, NGS genetic testing can be used to identify mutations in the SCN4A gene that may be responsible for the condition. By identifying these mutations, NGS genetic testing can help with the diagnosis of potassium-aggravated myotonia and provide important information for genetic counseling and treatment decisions. It can also be used for carrier testing in individuals with a family history of the condition.

Overall, the SCN4A gene potassium-aggravated myotonia NGS genetic test is a valuable tool in the diagnosis and management of this muscle disorder.

Test Name SCN4A Gene Potassium-aggravated myotonia 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 Potassium-aggravated myotonia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SCN4A Gene Potassium-aggravated myotonia
Test Details

The SCN4A gene is responsible for encoding a protein called the sodium channel voltage-gated type IV alpha subunit. Mutations in this gene can lead to a condition called potassium-aggravated myotonia.

Potassium-aggravated myotonia is a type of muscle disorder characterized by muscle stiffness and delayed relaxation after contraction. This condition is worsened by high levels of potassium in the blood, which can be triggered by factors such as exercise, stress, or certain medications.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes. In the case of potassium-aggravated myotonia, NGS genetic testing can be used to identify mutations in the SCN4A gene that may be responsible for the condition.

By identifying these mutations, NGS genetic testing can help with the diagnosis of potassium-aggravated myotonia and provide important information for genetic counseling and treatment decisions. It can also be used for carrier testing in individuals with a family history of the condition.

Overall, the SCN4A gene potassium-aggravated myotonia NGS genetic test is a valuable tool in the diagnosis and management of this muscle disorder.

SKU: TEST-1935 Category:

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