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CHAT Gene Myasthenic Syndrome Congenital Genetic Test Cost

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

-21%

The CHAT Gene Myasthenic Syndrome Congenital Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the CHAT gene, which are known to cause Congenital Myasthenic Syndrome (CMS). CMS is a group of inherited neuromuscular disorders characterized by muscle weakness and fatigue, with symptoms often appearing at birth or early childhood. The CHAT gene plays a crucial role in the synthesis of acetylcholine, a neurotransmitter essential for muscle contraction. Mutations in this gene can disrupt normal neuromuscular junction function, leading to the symptoms observed in CMS.

This genetic test involves analyzing the patient’s DNA to identify any mutations in the CHAT gene that may be responsible for the condition. It is a vital tool for confirming a diagnosis of CMS, enabling early and accurate identification of the disorder. Early diagnosis is critical for managing symptoms, improving quality of life, and preventing complications.

The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. DNA Labs UAE employs state-of-the-art technology and follows strict quality control measures to ensure accurate and reliable test results. The cost of the CHAT Gene Myasthenic Syndrome Congenital Genetic Test at DNA Labs UAE is 4400 AED. This investment in health can provide essential information for affected individuals and their families, guiding treatment decisions and genetic counseling.

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CHAT Gene Myasthenic Syndrome Congenital Genetic Test

Test Name: CHAT Gene Myasthenic Syndrome Congenital 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: Clinical History of Patient who is going for CHAT Gene Myasthenic Syndrome Congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CHAT Gene Myasthenic Syndrome Congenital.

Test Details

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It is a powerful tool for diagnosing genetic disorders, including gene myasthenic syndrome, congenital.

Gene myasthenic syndrome, congenital is a group of genetic disorders characterized by muscle weakness and fatigue. It is caused by mutations in genes involved in the neuromuscular junction, which is the connection between nerve cells and muscles.

NGS genetic testing can identify specific mutations in the genes associated with gene myasthenic syndrome, congenital. By analyzing the DNA sequence of these genes, the test can determine if any disease-causing mutations are present.

The benefits of NGS genetic testing for gene myasthenic syndrome, congenital include:

  1. Comprehensive analysis: NGS can simultaneously analyze multiple genes associated with the syndrome, providing a more comprehensive evaluation compared to traditional genetic testing methods.
  2. High accuracy: NGS has high sensitivity and specificity, allowing for the detection of even rare mutations associated with gene myasthenic syndrome, congenital.
  3. Faster results: NGS testing is faster compared to traditional genetic testing methods, enabling quicker diagnosis and potentially earlier intervention and treatment.
  4. Cost-effective: NGS can analyze multiple genes in a single test, which can be more cost-effective compared to testing each gene individually.

It is important to note that NGS genetic testing should be performed by a qualified geneticist or genetic counselor who can interpret the results accurately and provide appropriate counseling and guidance.

Overall, NGS genetic testing is a valuable tool for diagnosing gene myasthenic syndrome, congenital and can help guide treatment decisions and management strategies for affected individuals.

Test Name CHAT Gene Myasthenic syndrome congenital 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 CHAT Gene Myasthenic syndrome, congenital NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CHAT Gene Myasthenic syndrome, congenital
Test Details

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It is a powerful tool for diagnosing genetic disorders, including gene myasthenic syndrome, congenital.

Gene myasthenic syndrome, congenital is a group of genetic disorders characterized by muscle weakness and fatigue. It is caused by mutations in genes involved in the neuromuscular junction, which is the connection between nerve cells and muscles.

NGS genetic testing can identify specific mutations in the genes associated with gene myasthenic syndrome, congenital. By analyzing the DNA sequence of these genes, the test can determine if any disease-causing mutations are present.

The benefits of NGS genetic testing for gene myasthenic syndrome, congenital include:

1. Comprehensive analysis: NGS can simultaneously analyze multiple genes associated with the syndrome, providing a more comprehensive evaluation compared to traditional genetic testing methods.

2. High accuracy: NGS has high sensitivity and specificity, allowing for the detection of even rare mutations associated with gene myasthenic syndrome, congenital.

3. Faster results: NGS testing is faster compared to traditional genetic testing methods, enabling quicker diagnosis and potentially earlier intervention and treatment.

4. Cost-effective: NGS can analyze multiple genes in a single test, which can be more cost-effective compared to testing each gene individually.

It is important to note that NGS genetic testing should be performed by a qualified geneticist or genetic counselor who can interpret the results accurately and provide appropriate counseling and guidance.

Overall, NGS genetic testing is a valuable tool for diagnosing gene myasthenic syndrome, congenital and can help guide treatment decisions and management strategies for affected individuals.

SKU: TEST-1772 Category:

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