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NDUFS7 Gene Leigh syndrome Genetic Test

4,400 د.إ

-21%

The NDUFS7 Gene Leigh Syndrome Genetic Test is a specialized diagnostic examination available at DNA Labs UAE, designed to detect mutations in the NDUFS7 gene that are associated with Leigh syndrome, a severe neurological disorder. Leigh syndrome, also known as subacute necrotizing encephalomyelopathy, is a progressive disease characterized by the degeneration of the central nervous system. It is genetically heterogeneous, meaning it can be caused by mutations in various genes, including NDUFS7, which plays a crucial role in mitochondrial function and energy production.

The test is particularly important for individuals with a family history of Leigh syndrome or those showing symptoms of the disease, such as developmental delay, muscle weakness, and difficulties with movement and breathing. Early and accurate diagnosis through the NDUFS7 Gene Leigh Syndrome Genetic Test can lead to better management of symptoms and improved quality of life for affected individuals.

Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers a reliable analysis of the NDUFS7 gene. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations associated with the condition. This genetic test represents a critical step towards personalized medicine, enabling tailored treatment plans based on an individual’s genetic makeup, and providing families with essential information about the inheritance pattern and risks of Leigh syndrome.

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NDUFS7 Gene Leigh Syndrome Genetic Test

Overview

The NDUFS7 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. This syndrome is characterized by progressive neurological deterioration, including developmental delay, loss of motor skills, muscle weakness, and respiratory problems.

Test Details

The NDUFS7 Gene Leigh Syndrome Genetic Test is a neurologically focused genetic test that utilizes Next-Generation Sequencing (NGS) technology. This test analyzes the NDUFS7 gene to identify any mutations or variants that may be present. By analyzing this gene, healthcare professionals can provide valuable information about the genetic cause of Leigh syndrome, aiding in diagnosis and treatment planning.

Components and Price

  • Test Name: NDUFS7 Gene Leigh Syndrome Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED

Sample Condition

Patients can provide a blood sample, extracted DNA, or one drop of blood on an FTA Card for this test.

Report Delivery

The test results will be delivered within 3 to 4 weeks.

Doctor and Test Department

This test is conducted by a Neurologist in the Genetics department.

Pre Test Information

Prior to the test, a Genetic Counselling session is recommended. This session helps in drawing a pedigree chart of family members affected by NDUFS7 Gene Leigh syndrome, providing important insights into the genetic history of the disorder.

Interpreting the Results

It is important to note that NGS genetic testing may not be available in all healthcare facilities and may require a referral to a specialized genetics center or laboratory. Additionally, genetic testing results should always be interpreted in conjunction with a thorough clinical evaluation and consultation with a healthcare professional or genetic counselor.

Conclusion

The NDUFS7 Gene Leigh Syndrome Genetic Test using NGS technology offers valuable insights into the genetic cause of Leigh syndrome. By identifying specific genetic mutations or variants, healthcare professionals can confirm a diagnosis, provide accurate genetic counseling, and guide treatment decisions.

Test Name NDUFS7 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 NDUFS7 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS7 Gene Leigh syndrome
Test Details

The NDUFS7 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 developmental delay, loss of motor skills, muscle weakness, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the NDUFS7 gene and identify any mutations or variants that may be present. This type of testing can provide valuable information about the genetic cause of Leigh syndrome and help with diagnosis and treatment planning.

By analyzing the NDUFS7 gene using NGS, healthcare professionals can identify specific genetic mutations or variants that may be responsible for Leigh syndrome. This information can be used to confirm a diagnosis, provide accurate genetic counseling, and potentially guide treatment decisions.

It is important to note that NGS genetic testing may not be available in all healthcare facilities and may require a referral to a specialized genetics center or laboratory. Additionally, genetic testing results should always be interpreted in conjunction with a thorough clinical evaluation and consultation with a healthcare professional or genetic counselor.