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FOXRED1 Gene Leigh syndrome Genetic Test

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

-21%

The FOXRED1 Gene Leigh Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the FOXRED1 gene, which are linked to Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically emerges in the first year of life, characterized by progressive loss of mental and movement abilities. The test plays a crucial role in the early detection and management of this condition, allowing for personalized treatment plans that can significantly improve the quality of life for affected individuals. Priced at 4400 AED, this genetic test provides families with crucial information regarding the genetic underpinnings of Leigh syndrome, enabling informed decisions about care and support.

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FOXRED1 Gene Leigh syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer the FOXRED1 Gene Leigh syndrome Genetic Test. This test can help diagnose Leigh syndrome, a rare genetic disorder affecting the central nervous system.

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 the FOXRED1 Gene Leigh syndrome NGS Genetic DNA 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 by FOXRED1 Gene Leigh syndrome.

Test Details

The FOXRED1 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. Symptoms of Leigh syndrome include progressive loss of motor and cognitive abilities, muscle weakness, seizures, and respiratory problems.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the FOXRED1 gene. By using NGS, we can identify mutations or changes in the DNA sequence of the FOXRED1 gene that may be responsible for Leigh syndrome.

The FOXRED1 gene provides instructions for making a protein involved in the function of mitochondria, which are responsible for producing energy in cells. Mutations in the FOXRED1 gene can disrupt the normal functioning of mitochondria, leading to the symptoms associated with Leigh syndrome.

NGS genetic testing for FOXRED1 gene mutations can help confirm a diagnosis of Leigh syndrome and provide information about the specific genetic changes that are contributing to the disorder. This information can be useful for understanding the underlying cause of the disease, predicting disease progression, and potentially guiding treatment options.

Test Name FOXRED1 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 FOXRED1 Gene Leigh syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FOXRED1 Gene Leigh syndrome
Test Details

The FOXRED1 gene is associated with Leigh syndrome, a rare genetic disorder that affects the central nervous system. Leigh syndrome is characterized by progressive loss of motor and cognitive abilities, muscle weakness, seizures, and respiratory problems.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the FOXRED1 gene. NGS can identify mutations or changes in the DNA sequence of the FOXRED1 gene that may be responsible for Leigh syndrome.

The FOXRED1 gene provides instructions for making a protein involved in the function of mitochondria, which are responsible for producing energy in cells. Mutations in the FOXRED1 gene can disrupt the normal functioning of mitochondria, leading to the symptoms associated with Leigh syndrome.

NGS genetic testing for FOXRED1 gene mutations can help confirm a diagnosis of Leigh syndrome and provide information about the specific genetic changes that are contributing to the disorder. This information can be useful for understanding the underlying cause of the disease, predicting disease progression, and potentially guiding treatment options.