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MT-TV Gene Neonatal Death Due Leigh Syndrome MT-TV Related Genetic Test Cost

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

-21%

The MT-TV gene is associated with a mitochondrial condition that can lead to Leigh Syndrome, a severe neurological disorder that typically manifests in infancy. This syndrome is characterized by progressive loss of mental and movement abilities, which can lead to early death, often within the first few years of life. The condition is linked to defects in mitochondrial DNA, where the MT-TV gene plays a crucial role in protein synthesis within the mitochondria, essential for energy production in cells.

To identify the potential risk or presence of Leigh Syndrome associated with mutations in the MT-TV gene, DNA Labs UAE offers a specialized genetic test. This test is crucial for early detection, allowing for timely intervention and management of the condition to improve the quality of life for affected individuals. The genetic test involves analyzing the patient’s DNA to identify mutations in the MT-TV gene that are known to cause Leigh Syndrome.

The cost of the MT-TV gene-related genetic test for neonatal death due to Leigh Syndrome at DNA Labs UAE is 4400 AED. This price includes the collection of a DNA sample, usually through a blood draw or cheek swab, and comprehensive analysis by the laboratory. Results from this test can provide essential information for families with a history of Leigh Syndrome or those who have had children with unexplained neonatal death, guiding future family planning and potential treatments.

Given the complexity and potential impact of the results, genetic counseling is often recommended alongside the test. This counseling provides individuals and families with information about the implications of the test results, the nature of Leigh Syndrome, and support for dealing with the outcomes of the genetic testing.

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MT-TV Gene Neonatal Death Due to Leigh Syndrome MT-TV Related Genetic Test

At DNA Labs UAE, we offer the MT-TV Gene Neonatal Death Due to Leigh Syndrome MT-TV Related Genetic Test. This test is designed to diagnose Leigh syndrome, a rare genetic disorder characterized by progressive neurological deterioration that typically appears in infancy or early childhood.

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 MT-TV Gene Neonatal Death Due to Leigh Syndrome MT-TV Related 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 by MT-TV Gene Neonatal Death Due to Leigh Syndrome MT-TV Related.

Test Details

The MT-TV gene is associated with Leigh syndrome, a severe genetic disorder that causes progressive neurological deterioration. Neonatal death due to Leigh syndrome refers to the unfortunate outcome of the disorder occurring within the first few weeks or months of life. Our NGS genetic testing method allows for the simultaneous analysis of multiple genes, including the MT-TV gene, to identify mutations or variations associated with Leigh syndrome.

To perform the test, a DNA sample is required, usually obtained through a blood sample. The DNA is then sequenced using NGS technology, comparing the sequencing data to a reference genome to identify any mutations or variations in the MT-TV gene or other relevant genes associated with Leigh syndrome.

The results of the NGS genetic test can confirm a diagnosis of Leigh syndrome, providing valuable information for genetic counseling, family planning, and potential treatment options. It is important to note that while genetic testing can be helpful, it may not always provide definitive answers or a cure for the condition.

Test Name MT-TV Gene Neonatal death due Leigh syndrome MT-TV related 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 MT-TV Gene Neonatal death due Leigh syndrome, MT-TV related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-TV Gene Neonatal death due Leigh syndrome, MT-TV related
Test Details

MT-TV gene is associated with a rare genetic disorder called Leigh syndrome, which is characterized by progressive neurological deterioration typically appearing in infancy or early childhood. Leigh syndrome is caused by mutations in mitochondrial genes, including the MT-TV gene.

Neonatal death due to Leigh syndrome refers to the unfortunate outcome of the disorder occurring in the first few weeks or months of life. It is a severe form of the disease with rapid progression and poor prognosis.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and identify mutations or variations that may be associated with a particular disorder. In the case of Leigh syndrome, an NGS genetic test can help identify mutations in the MT-TV gene or other mitochondrial genes, providing a diagnosis for the condition.

This genetic test involves obtaining a DNA sample, usually through a blood sample, from the individual being tested. The DNA is then sequenced using NGS technology, which allows for the simultaneous analysis of multiple genes. The sequencing data is then compared to a reference genome to identify any mutations or variations in the MT-TV gene or other relevant genes associated with Leigh syndrome.

The results of the NGS genetic test can help confirm a diagnosis of Leigh syndrome and provide valuable information for genetic counseling, family planning, and potential treatment options. It is important to note that while genetic testing can be helpful, it may not always provide definitive answers or a cure for the condition.

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