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DOK7 Gene Myasthenic Syndrome Congenital Type 10 Genetic Test Cost

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

-21%

DOK7 Gene Myasthenic Syndrome Congenital Type 10 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the DOK7 gene, which are implicated in causing Congenital Myasthenic Syndrome Type 10 (CMS10). CMS10 is a rare genetic disorder characterized by muscle weakness and fatigue, which can significantly impact an individual’s quality of life. The test aims to provide definitive genetic evidence of the condition, aiding in the accurate diagnosis and management of the syndrome.

The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for any genetic abnormalities in the DOK7 gene. Early diagnosis through this genetic test can be crucial for the effective treatment and management of symptoms, including tailored therapies and interventions that can improve patient outcomes.

The cost of the DOK7 Gene Myasthenic Syndrome Congenital Type 10 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis and the provision of a detailed report, which is invaluable for individuals suspected of having CMS10, as well as for their families and healthcare providers. By confirming the genetic basis of the condition, this test plays a pivotal role in guiding treatment decisions and offers insight into the prognosis and potential genetic counseling needs of affected families.

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DOK7 Gene Myasthenic Syndrome Congenital Type 10 Genetic Test

Welcome to DNA Labs UAE, where we offer the DOK7 Gene Myasthenic Syndrome Congenital Type 10 Genetic Test. This test is designed to diagnose and manage a rare genetic disorder that affects the neuromuscular junction, resulting in muscle weakness and fatigue.

Test Components

The DOK7 Gene Myasthenic Syndrome Congenital Type 10 Genetic Test includes the following 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 DOK7 Gene Myasthenic Syndrome Congenital Type 10 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 this genetic disorder.

Test Details

The DOK7 gene myasthenic syndrome, congenital, type 10 is a rare genetic disorder that affects the neuromuscular junction. It is caused by mutations in the DOK7 gene, which plays a role in the formation and maintenance of the neuromuscular junction.

NGS (Next-Generation Sequencing) genetic testing is a diagnostic tool used to identify mutations or changes in genes that may be responsible for a particular disorder or condition. In the case of DOK7 gene myasthenic syndrome, congenital, type 10, NGS genetic testing can be used to analyze the DOK7 gene and identify any mutations or variants that may be present.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any differences. This can help determine if there are any mutations or variants in the DOK7 gene associated with the development of the disorder.

NGS genetic testing can be useful in confirming a diagnosis of DOK7 gene myasthenic syndrome, congenital, type 10, especially in cases where the clinical presentation is unclear or atypical. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families with a known DOK7 gene mutation.

Overall, NGS genetic testing for DOK7 gene myasthenic syndrome, congenital, type 10 can provide valuable information for diagnosis, genetic counseling, and management of the condition.

Test Name DOK7 Gene Myasthenic syndrome congenital type 10 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 DOK7 Gene Myasthenic syndrome, congenital, type 10 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DOK7 Gene Myasthenic syndrome, congenital, type 10
Test Details

DOK7 gene myasthenic syndrome, congenital, type 10 is a rare genetic disorder that affects the neuromuscular junction, resulting in muscle weakness and fatigue. It is caused by mutations in the DOK7 gene, which is involved in the formation and maintenance of the neuromuscular junction.

NGS (Next-Generation Sequencing) genetic testing is a diagnostic tool used to identify mutations or changes in genes that may be responsible for a particular disorder or condition. In the case of DOK7 gene myasthenic syndrome, congenital, type 10, NGS genetic testing can be used to analyze the DOK7 gene and identify any mutations or variants that may be present.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome to identify any differences. This can help to determine if there are any mutations or variants in the DOK7 gene that are associated with the development of the disorder.

NGS genetic testing can be useful in confirming a diagnosis of DOK7 gene myasthenic syndrome, congenital, type 10, particularly in cases where the clinical presentation is unclear or atypical. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families with a known DOK7 gene mutation.

Overall, NGS genetic testing for DOK7 gene myasthenic syndrome, congenital, type 10 can provide valuable information for diagnosis, genetic counseling, and management of the condition.