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BCS1L Gene Leigh syndrome Genetic Test

4,400 د.إ

-21%

The BCS1L gene Leigh syndrome genetic test is a specialized diagnostic examination aimed at detecting mutations in the BCS1L gene, which are associated with Leigh syndrome, a severe neurological disorder. This test is particularly important for families with a history of the condition or for individuals showing symptoms related to Leigh syndrome, such as developmental delay, movement disorders, and degeneration of the central nervous system. Conducted at DNA Labs UAE, a leading facility in genetic testing, this test provides crucial information that can aid in the diagnosis, management, and understanding of Leigh syndrome. The cost of the test is 4400 AED, reflecting the intricate technology and expertise required to accurately identify mutations in the BCS1L gene and provide individuals and families with essential genetic insights.

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BCS1L Gene Leigh syndrome Genetic Test

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

Clinical History of Patient who is going for BCS1L Gene Leigh syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BCS1L Gene Leigh syndrome.

Test Details

The BCS1L gene is associated with a rare genetic disorder called Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically presents in infancy or early childhood and is characterized by progressive loss of mental and movement abilities. It is caused by mutations in various genes, including BCS1L.

Next-generation sequencing (NGS) is a genetic testing method that allows for the analysis of multiple genes simultaneously. In the context of Leigh syndrome, NGS can be used to identify mutations in the BCS1L gene or other genes associated with the disorder. This can help in confirming a diagnosis, predicting the prognosis, and providing genetic counseling to affected individuals and their families.

The BCS1L gene Leigh syndrome NGS genetic test involves obtaining a DNA sample, usually through a blood sample, from the individual suspected of having Leigh syndrome. The DNA is then sequenced using NGS technology to identify any mutations or variations in the BCS1L gene. The results of the test can help guide treatment decisions and provide information about the risk of passing on the condition to future generations.

It is important to note that genetic testing for Leigh syndrome and other genetic disorders should be conducted by a qualified healthcare professional or genetic counselor. They can provide appropriate counseling and support throughout the testing process and help interpret the results.

Test Name BCS1L Gene Leigh syndrome 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 BCS1L Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with BCS1L Gene Leigh syndrome
Test Details

The BCS1L gene is associated with a rare genetic disorder called Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically presents in infancy or early childhood and is characterized by progressive loss of mental and movement abilities. It is caused by mutations in various genes, including BCS1L.

Next-generation sequencing (NGS) is a genetic testing method that allows for the analysis of multiple genes simultaneously. In the context of Leigh syndrome, NGS can be used to identify mutations in the BCS1L gene or other genes associated with the disorder. This can help in confirming a diagnosis, predicting the prognosis, and providing genetic counseling to affected individuals and their families.

The BCS1L gene Leigh syndrome NGS genetic test involves obtaining a DNA sample, usually through a blood sample, from the individual suspected of having Leigh syndrome. The DNA is then sequenced using NGS technology to identify any mutations or variations in the BCS1L gene. The results of the test can help guide treatment decisions and provide information about the risk of passing on the condition to future generations.

It is important to note that genetic testing for Leigh syndrome and other genetic disorders should be conducted by a qualified healthcare professional or genetic counselor. They can provide appropriate counseling and support throughout the testing process and help interpret the results.