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MT-ND5 Gene Leigh syndrome due to mitochondrial complex I deficiency Genetic Test

4,400 د.إ

-21%

The MT-ND5 gene Leigh syndrome due to mitochondrial complex I deficiency is a genetic condition that affects the nervous system and other bodily functions. This condition is caused by mutations in the MT-ND5 gene, which is part of the mitochondrial DNA. These mutations lead to a deficiency in mitochondrial complex I, a crucial component of the mitochondrial respiratory chain responsible for energy production in cells. Symptoms of Leigh syndrome can include developmental delay, muscle weakness, breathing difficulties, and neurological problems.

To diagnose this specific form of Leigh syndrome, a genetic test is available at DNA Labs UAE. This test specifically looks for mutations in the MT-ND5 gene to confirm a diagnosis of Leigh syndrome due to mitochondrial complex I deficiency. The test is crucial for accurate diagnosis and management of the condition, allowing for tailored treatment plans and genetic counseling for affected families.

The cost of the MT-ND5 gene Leigh syndrome genetic test at DNA Labs UAE is 4400 AED. This investment covers the process of collecting a DNA sample, usually through a blood draw or cheek swab, and the detailed analysis conducted in the laboratory to detect any mutations in the MT-ND5 gene. Given the complexity of the test and the specialized technology used, the cost reflects the extensive resources required for accurate diagnosis.

For families and individuals facing symptoms indicative of Leigh syndrome, this genetic test provides a vital tool for understanding the underlying genetic cause and opens the door to targeted interventions and support services.

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MT-ND5 Gene Leigh Syndrome Genetic Test

Are you concerned about Leigh syndrome due to mitochondrial complex I deficiency? DNA Labs UAE offers the MT-ND5 Gene Leigh syndrome genetic test to provide you with valuable insights into this genetic disorder. Read on to learn more about this test.

Test Details

The MT-ND5 gene Leigh syndrome is a severe neurological disorder caused by mutations in the MT-ND5 gene, which is part of the mitochondrial DNA. This gene plays a crucial role in the energy production process in cells by providing instructions for making a protein that is a subunit of complex I. Leigh syndrome typically manifests in infancy or early childhood and is characterized by progressive loss of mental and movement abilities, muscle weakness, poor coordination, seizures, and respiratory problems. Symptoms can vary but generally worsen over time and can be life-threatening.

Test Components and Price

  • Test Name: MT-ND5 Gene Leigh syndrome due to mitochondrial complex I deficiency Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED

Sample Condition and Report Delivery

You can provide a blood sample, extracted DNA, or one drop of blood on an FTA Card for this test. The report will be delivered to you within 3 to 4 weeks.

Test Type and Doctor

The MT-ND5 Gene Leigh syndrome genetic test falls under the category of Neurological Disorders. It is recommended to consult with a Neurologist for this test.

Test Department

This test is conducted in the Genetics department of DNA Labs UAE.

Pre Test Information

Before undergoing the MT-ND5 Gene Leigh syndrome genetic test, it is essential 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-ND5 Gene Leigh syndrome due to mitochondrial complex I deficiency.

About NGS Technology

NGS (Next-Generation Sequencing) is a state-of-the-art DNA sequencing technology that allows for the simultaneous analysis of multiple genes. This comprehensive approach provides a detailed view of an individual’s genetic makeup. In the context of Leigh syndrome due to mitochondrial complex I deficiency, NGS genetic testing can identify mutations in the MT-ND5 gene or other genes associated with mitochondrial complex I deficiency.

The Testing Process

The MT-ND5 Gene Leigh syndrome genetic test involves obtaining a DNA sample, usually through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the MT-ND5 gene or other relevant genes. The test results can confirm a diagnosis of Leigh syndrome and provide information about the specific genetic mutation involved.

Benefits of Genetic Testing

Genetic testing can be instrumental in diagnosing Leigh syndrome and assessing the risk of passing on the condition to future generations. It can also aid in treatment decisions, provide insights into prognosis, and identify potential complications. However, it is important to note that genetic testing cannot cure Leigh syndrome or reverse its symptoms. Treatment typically focuses on symptom management and supportive care.

If you suspect Leigh syndrome due to mitochondrial complex I deficiency, the MT-ND5 Gene Leigh syndrome genetic test can provide you with valuable information. Contact DNA Labs UAE today to schedule your test.

Test Name MT-ND5 Gene Leigh syndrome due to mitochondrial complex I deficiency 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-ND5 Gene Leigh syndrome due to mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND5 Gene Leigh syndrome due to mitochondrial complex I deficiency
Test Details

MT-ND5 gene Leigh syndrome is a genetic disorder caused by mutations in the MT-ND5 gene, which is a part of the mitochondrial DNA. This gene provides instructions for making a protein that is a subunit of complex I, which is involved in the energy production process in cells.

Leigh syndrome is a severe neurological disorder that typically begins in infancy or early childhood. It is characterized by progressive loss of mental and movement abilities, muscle weakness, poor coordination, seizures, and respiratory problems. The symptoms of Leigh syndrome can vary widely, but they generally worsen over time and can be life-threatening.

NGS (Next-Generation Sequencing) genetic testing is a type of DNA sequencing technology that can analyze multiple genes simultaneously, providing a comprehensive view of an individual’s genetic makeup. In the context of Leigh syndrome due to mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations in the MT-ND5 gene or other genes associated with mitochondrial complex I deficiency.

The NGS genetic test for Leigh syndrome due to mitochondrial complex I deficiency typically involves obtaining a DNA sample, usually through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the MT-ND5 gene or other relevant genes. The results of the test can help confirm a diagnosis of Leigh syndrome and provide information about the specific genetic mutation involved.

Genetic testing can be useful in diagnosing Leigh syndrome and determining the risk of passing on the condition to future generations. It can also help guide treatment decisions and provide information about prognosis and potential complications. However, it is important to note that genetic testing cannot cure Leigh syndrome or reverse its symptoms. Treatment for Leigh syndrome is generally focused on managing symptoms and providing supportive care.