CNNM2 Gene Hypomagnesemia Type 6 NGS Genetic DNA Test
Comprehensive Genetic Testing for Magnesium Metabolism Disorders
The CNNM2 Gene Hypomagnesemia Type 6 NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for magnesium metabolism disorders. This advanced test specifically targets the CNNM2 gene, which plays a critical role in magnesium homeostasis and cellular magnesium transport. Hypomagnesemia type 6 is a rare autosomal recessive condition characterized by severe magnesium deficiency that can lead to significant neurological and metabolic complications if left undiagnosed.
What Does This Test Measure?
Our comprehensive NGS-based genetic test analyzes the complete coding region of the CNNM2 gene to identify pathogenic variants responsible for hypomagnesemia type 6. The test specifically detects:
- Point mutations in the CNNM2 gene coding sequence
- Small insertions and deletions affecting gene function
- Copy number variations impacting gene dosage
- Splice site mutations that disrupt normal protein production
- Novel variants with potential clinical significance
Who Should Consider This Test?
This genetic test is recommended for individuals presenting with:
- Unexplained persistent hypomagnesemia despite adequate dietary intake
- Neurological symptoms including seizures, muscle weakness, or tremors
- Family history of magnesium metabolism disorders
- Early-onset magnesium deficiency in childhood or adolescence
- Renal magnesium wasting without apparent cause
- Developmental delays associated with electrolyte imbalances
- Cardiac arrhythmias linked to magnesium deficiency
Clinical Benefits of Genetic Testing
Undergoing CNNM2 gene testing provides numerous clinical advantages:
- Accurate Diagnosis: Confirms or rules out hypomagnesemia type 6 with high precision
- Personalized Treatment: Enables targeted magnesium supplementation strategies
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Early Intervention: Facilitates proactive management to prevent complications
- Differential Diagnosis: Helps distinguish between various forms of hereditary hypomagnesemia
- Long-term Monitoring: Establishes baseline for ongoing clinical management
Understanding Your Test Results
Our comprehensive genetic report provides clear interpretation of your results:
- Positive Result: Identifies pathogenic variants in the CNNM2 gene, confirming diagnosis of hypomagnesemia type 6
- Negative Result: No disease-causing variants detected, suggesting alternative causes for symptoms
- Variant of Uncertain Significance: Identifies genetic changes requiring further clinical correlation
- Carrier Status: Identifies individuals with single copy of mutated gene who may pass condition to offspring
Test Details and Pricing
| Test Component | Details |
|---|---|
| Test Name | CNNM2 Gene Hypomagnesemia Type 6 NGS Genetic DNA Test |
| Regular Price | $700 USD |
| Discount Price | $500 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
| Testing Method | Next-Generation Sequencing (NGS) Technology |
| Specialty | Genetics and Metabolic Disorders |
Pre-Test Requirements
Before scheduling your test, we recommend:
- Comprehensive clinical history documentation
- Genetic counseling session to create detailed family pedigree
- Review of previous magnesium level testing results
- Discussion of potential implications for family members
Nationwide Testing Availability
We provide comprehensive genetic testing services across the United States with convenient locations in major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art laboratories ensure consistent, high-quality results regardless of your location.
Take Control of Your Health Today
Don’t let unexplained symptoms or family history of magnesium disorders remain a mystery. Our CNNM2 Gene Hypomagnesemia Type 6 NGS Genetic DNA Test provides the clarity you need for proper diagnosis and management. With our discounted price of $500 USD, advanced genetic testing is more accessible than ever.
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.
Our experienced genetic counselors are available to discuss your specific concerns, explain the testing process, and help you make informed decisions about your healthcare journey. Early diagnosis through genetic testing can significantly improve quality of life and prevent serious complications associated with magnesium metabolism disorders.
