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NDUFA10 Gene Leigh syndrome Genetic Test

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

-21%

The NDUFA10 gene is associated with a condition known as Leigh syndrome, a severe neurological disorder that typically arises in the first year of life. This condition is characterized by progressive loss of mental and movement abilities, which can lead to severe physical and mental disabilities. The NDUFA10 gene plays a crucial role in the mitochondrial function, which is vital for energy production in cells. Mutations in this gene can disrupt normal mitochondrial function, leading to the symptoms observed in Leigh syndrome.

To diagnose this condition accurately and to guide treatment options, genetic testing for mutations in the NDUFA10 gene is available. DNA Labs UAE offers a specialized genetic test designed to identify mutations in the NDUFA10 gene that are linked to Leigh syndrome. This test is crucial for families seeking answers about this condition, allowing for early intervention and management strategies that can improve quality of life.

The cost of the NDUFA10 Gene Leigh Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is performed with high precision and accuracy, providing essential information for affected individuals and their families. The testing process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic mutations associated with Leigh syndrome. The results from this test can help guide clinical decisions, including treatment and management plans, and provide valuable information for genetic counseling.

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NDUFA10 Gene Leigh Syndrome Genetic Test

Introduction

The NDUFA10 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. This blog will provide detailed information about the NDUFA10 Gene Leigh Syndrome Genetic Test offered by DNA Labs UAE.

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

Prior to undergoing the NDUFA10 Gene Leigh Syndrome 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 NDUFA10 Gene Leigh Syndrome.

Test Details

Leigh syndrome is characterized by progressive neurological deterioration, including muscle weakness, movement disorders, seizures, and respiratory problems. The NDUFA10 gene is associated with this syndrome.

The NDUFA10 Gene Leigh Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology. This type of genetic testing allows for the simultaneous analysis of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. By analyzing the NDUFA10 gene, this test can identify mutations or variations that may be associated with Leigh syndrome.

In addition to diagnosing Leigh syndrome, this genetic test can also be used for carrier testing, prenatal testing, and family planning purposes.

It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor. These professionals can interpret the test results and provide appropriate recommendations and support.

Test Name NDUFA10 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 NDUFA10 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFA10 Gene Leigh syndrome
Test Details

The NDUFA10 gene is associated with Leigh syndrome, which is a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive neurological deterioration, including muscle weakness, movement disorders, seizures, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. NGS testing can be used to identify mutations or variations in the NDUFA10 gene that may be associated with Leigh syndrome.

The NGS genetic test for NDUFA10 gene mutations can help in diagnosing Leigh syndrome and determining the underlying cause of the condition. It can also be used for carrier testing, prenatal testing, and family planning purposes.

It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor, who can interpret the results and provide appropriate recommendations and support.