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NDUFS4 Gene Leigh syndrome Genetic Test

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

-21%

Leigh syndrome, a severe neurological disorder, is often linked to genetic mutations, one of which involves the NDUFS4 gene. This gene plays a crucial role in cellular energy production, and its mutations can lead to the development of Leigh syndrome, characterized by progressive loss of mental and movement abilities. To identify the presence of mutations in the NDUFS4 gene, DNA Labs UAE offers a specialized genetic test. This test is a critical tool for diagnosing Leigh syndrome, enabling early intervention and management of the condition. The cost of the NDUFS4 Gene Leigh Syndrome Genetic Test at DNA Labs UAE is 4400 AED. By providing accurate genetic diagnosis, this test is a cornerstone in the management and understanding of Leigh syndrome, offering hope and direction for affected families.

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NDUFS4 Gene Leigh Syndrome Genetic Test

Introduction

The NDUFS4 gene is associated with Leigh syndrome, a rare and severe neurological disorder. This blog will provide detailed information about the NDUFS4 Gene Leigh Syndrome Genetic Test offered by DNA Labs UAE, including its cost, symptoms, diagnosis, and more.

Test Details

The NDUFS4 Gene Leigh Syndrome Genetic Test is a comprehensive analysis of the NDUFS4 gene and other relevant genes associated with Leigh syndrome. It utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes or even the entire genome.

Symptoms and Diagnosis

Leigh syndrome is characterized by progressive loss of motor and mental abilities, muscle weakness, seizures, respiratory problems, and other symptoms. By analyzing the NDUFS4 gene through NGS genetic testing, any mutations or variations in the gene that may be contributing to the development of Leigh syndrome can be identified.

Test Components and Price

  • Test Name: NDUFS4 Gene Leigh Syndrome Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: 4400.0 AED

Sample Condition

The NDUFS4 Gene Leigh Syndrome Genetic Test requires a blood sample, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery

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

Test Type and Doctor

  • Test Type: Neurological Disorders
  • Doctor: Neurologist

Test Department

The NDUFS4 Gene Leigh Syndrome Genetic Test is conducted in the Genetics department.

Pre Test Information

Before undergoing the NDUFS4 Gene Leigh Syndrome Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by NDUFS4 Gene Leigh syndrome.

Conclusion

The NDUFS4 Gene Leigh Syndrome Genetic Test offered by DNA Labs UAE is a valuable tool for the diagnosis, prognosis, and genetic counseling of individuals and families affected by Leigh syndrome. By analyzing the NDUFS4 gene and other relevant genes through NGS technology, this test provides comprehensive insights into the development of Leigh syndrome and can guide treatment options and genetic counseling.

Test Name NDUFS4 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 NDUFS4 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with NDUFS4 Gene Leigh syndrome
Test Details

The NDUFS4 gene is associated with Leigh syndrome, which is a rare and severe neurological disorder. Leigh syndrome is characterized by progressive loss of motor and mental abilities, as well as other symptoms such as muscle weakness, seizures, and respiratory problems.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. This type of testing can provide a comprehensive analysis of the NDUFS4 gene and other relevant genes associated with Leigh syndrome.

By analyzing the NDUFS4 gene through NGS genetic testing, it is possible to identify any mutations or variations in the gene that may be contributing to the development of Leigh syndrome. This information can be useful for diagnosis, prognosis, and potentially for guiding treatment options or genetic counseling for affected individuals and their families.