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MT-TL1 Gene MELAS syndrome MT-TL1 related Genetic Test Cost

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

-21%

The MT-TL1 gene is associated with a condition known as MELAS syndrome, which stands for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes. This genetic disorder is characterized by a wide range of symptoms including muscle weakness, headaches, loss of appetite, seizures, and more. It is caused by mutations in the mitochondrial DNA, specifically in the MT-TL1 gene, which plays a crucial role in the production of transfer RNA (tRNA) for leucine, an essential component in the synthesis of proteins necessary for mitochondrial function.

To diagnose and assess the risk of MELAS syndrome, a genetic test targeting the MT-TL1 gene can be conducted. This test is crucial for individuals who exhibit symptoms of the syndrome or have a family history of mitochondrial disorders. It involves analyzing the DNA to identify mutations in the MT-TL1 gene that are known to cause the condition.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the MT-TL1 gene test for MELAS syndrome at DNA Labs UAE is 4400 AED. This comprehensive test is performed in a state-of-the-art laboratory by experienced geneticists and clinicians who ensure accurate and reliable results. The test not only aids in the diagnosis of MELAS syndrome but also helps in the management and treatment planning for affected individuals, offering them and their families essential information about the condition.

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MT-TL1 Gene MELAS Syndrome MT-TL1 Related Genetic Test

Components:

  • Test Name: MT-TL1 Gene MELAS syndrome MT-TL1 related Genetic Test
  • 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: Cardiovascular Pneumology Disorders
  • Doctor: Cardiologist
  • Test Department: Genetics
  • Pre Test Information: Clinical History of Patient who is going for MT-TL1 Gene MELAS syndrome, MT-TL1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TL1 Gene MELAS syndrome, MT-TL1 related NGS Genetic DNA Test gene MT-TL1

Test Details

MT-TL1 gene, also known as MT-TL1 transfer RNA (tRNA) gene, is associated with a mitochondrial disorder called MELAS syndrome. MELAS stands for Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes. MELAS syndrome is a rare genetic disorder that affects the mitochondria, which are the energy-producing structures within cells. It is caused by mutations in the MT-TL1 gene, which leads to impaired production of functional transfer RNA molecules.

The MT-TL1 related NGS (Next-Generation Sequencing) genetic test is a diagnostic tool used to detect mutations in the MT-TL1 gene. NGS technology allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of the genetic variations associated with MELAS syndrome. This genetic test involves collecting a sample of DNA, typically through a blood sample, and analyzing it to identify any mutations or variations in the MT-TL1 gene.

The results of the test can help confirm a diagnosis of MELAS syndrome and provide valuable information for managing the condition. It is important to note that MELAS syndrome is a complex disorder with various genetic causes. While mutations in the MT-TL1 gene are a common cause, other genes and factors can also contribute to the development of the condition. Therefore, a comprehensive genetic analysis may involve testing multiple genes associated with mitochondrial disorders.

Test Name MT-TL1 Gene MELAS syndrome MT-TL1 related 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 Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MT-TL1 Gene MELAS syndrome, MT-TL1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TL1 Gene MELAS syndrome, MT-TL1 related NGS Genetic DNA Test gene MT-TL1
Test Details

MT-TL1 gene, also known as MT-TL1 transfer RNA (tRNA) gene, is associated with a mitochondrial disorder called MELAS syndrome. MELAS stands for Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes.

MELAS syndrome is a rare genetic disorder that affects the mitochondria, which are the energy-producing structures within cells. It is caused by mutations in the MT-TL1 gene, which leads to impaired production of functional transfer RNA molecules.

The MT-TL1 related NGS (Next-Generation Sequencing) genetic test is a diagnostic tool used to detect mutations in the MT-TL1 gene. NGS technology allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of the genetic variations associated with MELAS syndrome.

This genetic test involves collecting a sample of DNA, typically through a blood sample, and analyzing it to identify any mutations or variations in the MT-TL1 gene. The results of the test can help confirm a diagnosis of MELAS syndrome and provide valuable information for managing the condition.

It is important to note that MELAS syndrome is a complex disorder with various genetic causes. While mutations in the MT-TL1 gene are a common cause, other genes and factors can also contribute to the development of the condition. Therefore, a comprehensive genetic analysis may involve testing multiple genes associated with mitochondrial disorders.

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