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

Original price was: $700.Current price is: $500.

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The MT-TV Gene Neonatal Death Due to Leigh Syndrome NGS Genetic DNA Test is a specialized diagnostic tool that identifies mutations in the MT-TV gene associated with Leigh syndrome, a severe neurological disorder. This comprehensive next-generation sequencing test provides crucial information for families affected by unexplained infant mortality or neurological deterioration. The test costs $500 USD and offers precise detection of mitochondrial DNA mutations that can cause progressive brain damage, developmental regression, and life-threatening complications in newborns and infants. Early identification through this test enables proactive medical management and informed family planning decisions.

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

Understanding MT-TV Gene and Leigh Syndrome

Leigh syndrome is a severe neurological disorder that typically manifests in infancy or early childhood, characterized by progressive brain damage that affects vital functions. The MT-TV gene, located in mitochondrial DNA, plays a critical role in energy production within cells. Mutations in this gene can disrupt mitochondrial function, leading to the devastating symptoms associated with Leigh syndrome.

This specialized genetic test represents a breakthrough in diagnostic precision for families facing unexplained infant neurological deterioration or mortality. By examining the MT-TV gene through advanced next-generation sequencing technology, we provide definitive answers that can guide treatment decisions and family planning.

What This Test Detects

The MT-TV Gene NGS Genetic DNA Test specifically identifies:

  • Pathogenic mutations in the mitochondrial MT-TV gene
  • Specific genetic variants associated with Leigh syndrome development
  • Mitochondrial DNA abnormalities affecting energy metabolism
  • Inheritance patterns of mitochondrial disorders
  • Risk assessment for future pregnancies

Who Should Consider This Test

This test is recommended for individuals and families experiencing:

  • Unexplained neonatal or infant death with neurological symptoms
  • Progressive neurological deterioration in infancy
  • Family history of Leigh syndrome or similar mitochondrial disorders
  • Infants showing developmental regression after initial normal development
  • Unexplained metabolic crises in newborns
  • Multiple affected siblings with neurological symptoms

Common Symptoms Indicating Need for Testing

  • Loss of previously acquired motor skills
  • Poor sucking ability and feeding difficulties
  • Seizures and involuntary muscle contractions
  • Respiratory problems and breathing irregularities
  • Weak muscle tone (hypotonia)
  • Vision and hearing impairment
  • Cardiovascular abnormalities

Benefits of MT-TV Gene Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Definitive Diagnosis: Obtain clear answers about the genetic cause of neurological symptoms
  • Family Planning Guidance: Understand inheritance risks for future pregnancies
  • Early Intervention: Enable prompt medical management and supportive care
  • Genetic Counseling: Receive expert guidance on implications for family members
  • Research Contribution: Help advance understanding of mitochondrial disorders
  • Peace of Mind: Reduce uncertainty and provide closure for affected families

Understanding Your Test Results

Our comprehensive genetic counseling services help you interpret your results:

Positive Result

A positive result indicates the presence of MT-TV gene mutations associated with Leigh syndrome. This confirmation enables:

  • Targeted medical management strategies
  • Family member screening recommendations
  • Reproductive planning options
  • Connection with support networks and specialized care

Negative Result

A negative result suggests that MT-TV gene mutations are not the cause of symptoms, allowing healthcare providers to:

  • Explore alternative diagnostic possibilities
  • Consider other mitochondrial or neurological disorders
  • Continue comprehensive medical evaluation

Variant of Uncertain Significance

Some results may identify genetic changes with unclear clinical implications. In such cases, we provide:

  • Detailed explanation of findings
  • Recommendations for additional testing if needed
  • Ongoing monitoring as research advances

Test Pricing Information

Price Type Amount (USD)
Discount Price $500
Regular Price $700

Nationwide Testing Availability

We have convenient testing locations across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, San Francisco, and many more. Our network of certified genetic counselors and medical professionals ensures you receive consistent, high-quality care regardless of location.

Take Action Today

Don’t let uncertainty about neurological symptoms in your family continue. Our expert team is ready to provide the answers and support you need. Schedule your MT-TV Gene Neonatal Death Due to Leigh Syndrome NGS Genetic DNA Test today by calling our dedicated genetic counseling hotline at +1(267) 388-9828 or booking your appointment online.

With a turnaround time of 3-4 weeks and comprehensive pre-test genetic counseling included, you’ll receive not just test results, but meaningful guidance and support throughout your diagnostic journey.