TMEM67 Gene Meckel Syndrome Type 3 NGS Genetic DNA Test
Comprehensive Genetic Analysis for Hereditary Disorders
The TMEM67 Gene Meckel Syndrome Type 3 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for rare hereditary conditions. This advanced testing methodology utilizes cutting-edge Next-Generation Sequencing technology to provide comprehensive analysis of the TMEM67 gene, which plays a critical role in cellular function and development. Meckel syndrome type 3 is a severe autosomal recessive disorder characterized by multiple congenital anomalies affecting vital organ systems.
What Does This Test Measure?
This sophisticated genetic test specifically targets and analyzes the TMEM67 gene for mutations and variants associated with Meckel syndrome type 3. The test detects:
- Point mutations and single nucleotide variants in the TMEM67 gene
- Insertions and deletions affecting gene function
- Copy number variations and structural abnormalities
- Pathogenic variants linked to hepatology, nephrology, and endocrinology disorders
- Inheritance patterns for family planning considerations
Who Should Consider This Test?
This genetic test is recommended for individuals and families experiencing specific clinical indications:
- Couples with family history of Meckel syndrome or related disorders
- Individuals presenting with congenital liver abnormalities
- Patients with renal cystic disease or kidney malformations
- Those experiencing endocrine system dysfunction
- Families with history of neonatal or infant mortality due to congenital anomalies
- Couples planning pregnancy with known genetic risk factors
- Individuals with unexplained developmental delays affecting multiple organ systems
Key Benefits of Genetic Testing
Undergoing the TMEM67 Gene Meckel Syndrome Type 3 test provides numerous advantages:
- Accurate Diagnosis: Precise identification of genetic mutations enables targeted medical management
- Family Planning Guidance: Understanding inheritance patterns helps in making informed reproductive decisions
- Early Intervention: Early detection allows for proactive medical care and monitoring
- Reduced Diagnostic Uncertainty: Eliminates prolonged diagnostic odysseys and unnecessary testing
- Personalized Treatment Approaches: Results guide specialized care for affected organ systems
- Genetic Counseling Support: Comprehensive interpretation and family risk assessment
Understanding Your Test Results
Our genetic counseling team provides detailed interpretation of your results:
- Positive Result: Indicates presence of pathogenic mutations requiring specialized medical follow-up
- Negative Result: Suggests absence of tested mutations, though other genetic factors may be considered
- Variant of Uncertain Significance: Requires additional family studies and clinical correlation
- Carrier Status: Identifies individuals who carry one copy of mutated gene without disease symptoms
All results are accompanied by comprehensive genetic counseling to ensure complete understanding and appropriate next steps.
Test Pricing and Details
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
Nationwide Testing Availability
We have comprehensive testing facilities across the United States, with branches in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network ensures accessible genetic testing services for patients nationwide.
Pre-Test Requirements
To ensure optimal testing outcomes, we recommend:
- Complete clinical history documentation
- Genetic counseling session to create detailed family pedigree
- Discussion of testing implications and potential outcomes
- Informed consent process
Take Control of Your Genetic Health Today
Don’t let uncertainty about genetic conditions affect your family’s future. Our TMEM67 Gene Meckel Syndrome Type 3 NGS Genetic DNA Test provides the clarity and information needed for informed healthcare decisions. With advanced NGS technology and expert genetic counseling, we deliver comprehensive genetic insights you can trust.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic test consultation and take the first step toward understanding your genetic health.
