BCS1L Gene GRACILE Syndrome Genetic Test sale cost 4400 AED
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BCS1L Gene GRACILE Syndrome Genetic Test Cost

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

-21%

The BCS1L Gene GRACILE Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the BCS1L gene, which are responsible for GRACILE Syndrome. GRACILE Syndrome is a rare genetic disorder characterized by growth retardation, aminoaciduria, cholestasis, iron overload, lactic acidosis, and early death. This condition is inherited in an autosomal recessive manner, meaning that both copies of the gene in each cell have mutations.

The test is particularly crucial for families with a history of the syndrome or individuals showing symptoms related to the condition. Early detection through this genetic test can lead to a better understanding of the disease, allowing for more targeted management and care strategies for affected individuals. The test involves analyzing the patient’s DNA to look for specific mutations in the BCS1L gene, which plays a crucial role in the normal function of mitochondria.

DNA Labs UAE offers this comprehensive genetic testing service for a cost of 4400 AED. The test is conducted in a state-of-the-art laboratory setting by experienced geneticists and technicians, ensuring high accuracy and reliability of the results. Upon completion, a detailed report is provided, offering insights into the presence of any genetic mutations associated with GRACILE Syndrome and guidance for further steps. This test is an invaluable tool for affected families, providing them with critical information for making informed health and lifestyle decisions.

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  • This test is not intended for medical diagnosis or treatment
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BCS1L Gene GRACILE Syndrome Genetic 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information:

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

Test Details:

The BCS1L gene is associated with GRACILE syndrome, which is a rare genetic disorder characterized by growth restriction, aminoaciduria, cholestasis (impaired bile flow), iron overload, lactic acidosis, and early death. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of genetic variations or mutations that may be responsible for a particular condition or disease. In the case of GRACILE syndrome, NGS genetic testing can be used to analyze the BCS1L gene for any mutations or variations that may be present. This type of genetic testing can provide valuable information for diagnosis, genetic counseling, and potentially guide treatment options for individuals with GRACILE syndrome. It is typically performed on a blood or saliva sample and involves sequencing the DNA to identify any genetic changes in the BCS1L gene.

Test Name BCS1L Gene GRACILE syndrome Genetic 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for BCS1L Gene GRACILE syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BCS1L Gene GRACILE syndrome NGS Genetic DNA Test gene BCS1L
Test Details

The BCS1L gene is associated with GRACILE syndrome, which is a rare genetic disorder characterized by growth restriction, aminoaciduria, cholestasis (impaired bile flow), iron overload, lactic acidosis, and early death.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of genetic variations or mutations that may be responsible for a particular condition or disease. In the case of GRACILE syndrome, NGS genetic testing can be used to analyze the BCS1L gene for any mutations or variations that may be present.

This type of genetic testing can provide valuable information for diagnosis, genetic counseling, and potentially guide treatment options for individuals with GRACILE syndrome. It is typically performed on a blood or saliva sample and involves sequencing the DNA to identify any genetic changes in the BCS1L gene.

SKU: TEST-4124