Sale!

MT-ND1 Gene Mitochondrial Complex I Deficiency Genetic Test

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

-21%

The “MT-ND1 Gene Mitochondrial Complex I Deficiency Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the MT-ND1 gene. This gene plays a crucial role in the proper functioning of Complex I, a key enzyme complex in the mitochondrial respiratory chain responsible for energy production in cells. Mutations in the MT-ND1 gene can lead to mitochondrial complex I deficiency, a condition that can cause a wide range of symptoms, including muscle weakness, neurological problems, and organ dysfunction. This genetic test is vital for the early detection and management of the condition, facilitating personalized treatment plans to improve patient outcomes. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the mitochondrial DNA. Conducted at DNA Labs UAE, this test represents a crucial step forward in the diagnosis and management of mitochondrial disorders, offering hope to affected individuals and their families.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

MT-ND1 Gene Mitochondrial Complex I Deficiency Genetic Test

Cost: 4400.0 AED

Symptoms, Diagnosis, and Test Details

The MT-ND1 gene is a gene found in the mitochondrial DNA (mtDNA) that encodes a subunit of complex I, which is a part of the electron transport chain in mitochondria. Mitochondrial complex I deficiency refers to a condition where there is a malfunction or reduced activity of complex I, leading to impaired energy production within cells.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variations in the MT-ND1 gene and other relevant genes that may be responsible for the condition.

By analyzing the patient’s DNA, NGS genetic testing can provide valuable information about the specific genetic variants present in the MT-ND1 gene and other genes associated with mitochondrial complex I deficiency. This information can help in diagnosing the condition, predicting disease progression, and guiding treatment decisions.

It is important to note that NGS genetic testing for mitochondrial complex I deficiency is typically performed in specialized laboratories or genetic testing centers, and the results should be interpreted by a qualified healthcare professional or genetic counselor. The results of the test can provide valuable insights into the genetic basis of the condition and may inform personalized treatment plans or management strategies.

Test Components

  • 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

Clinical History of Patient who is going for MT-ND1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND1 Gene Mitochondrial complex I deficiency

Test Name MT-ND1 Gene 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-ND1 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with MT-ND1 Gene Mitochondrial complex I deficiency
Test Details

The MT-ND1 gene is a gene found in the mitochondrial DNA (mtDNA) that encodes a subunit of complex I, which is a part of the electron transport chain in mitochondria. Mitochondrial complex I deficiency refers to a condition where there is a malfunction or reduced activity of complex I, leading to impaired energy production within cells.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of mitochondrial complex I deficiency, NGS genetic testing can be used to identify mutations or variations in the MT-ND1 gene and other relevant genes that may be responsible for the condition.

By analyzing the patient’s DNA, NGS genetic testing can provide valuable information about the specific genetic variants present in the MT-ND1 gene and other genes associated with mitochondrial complex I deficiency. This information can help in diagnosing the condition, predicting disease progression, and guiding treatment decisions.

It is important to note that NGS genetic testing for mitochondrial complex I deficiency is typically performed in specialized laboratories or genetic testing centers, and the results should be interpreted by a qualified healthcare professional or genetic counselor. The results of the test can provide valuable insights into the genetic basis of the condition and may inform personalized treatment plans or management strategies.