SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test
Comprehensive Genetic Testing for Manganese Metabolism Disorders
The SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying rare inherited metabolic disorders affecting manganese transport and metabolism. This specialized test utilizes next-generation sequencing technology to detect mutations in the SLC30A10 gene, which plays a critical role in manganese homeostasis within the body.
What This Advanced Genetic Test Detects
This comprehensive genetic analysis specifically targets mutations in the SLC30A10 gene that disrupt normal manganese transport mechanisms. The test identifies:
- Pathogenic variants in the SLC30A10 manganese transporter gene
- Genetic mutations causing abnormal manganese accumulation
- Inherited patterns of manganese metabolism disorders
- Specific genetic markers associated with neurological and hepatic complications
Who Should Consider This Genetic Test
This specialized genetic testing is recommended for individuals presenting with:
- Progressive movement disorders including dystonia and parkinsonism
- Unexplained polycythemia (elevated red blood cell counts)
- Early-onset liver cirrhosis without clear etiology
- Family history of similar neurological or metabolic conditions
- Developmental delays in childhood with movement abnormalities
- Elevated manganese levels detected in blood tests
Clinical Benefits of Genetic Testing
Undergoing the SLC30A10 genetic test provides numerous clinical advantages:
- Definitive diagnosis for complex neurological-metabolic presentations
- Accurate genetic counseling for family planning decisions
- Early intervention opportunities for affected family members
- Personalized treatment strategies based on genetic findings
- Clear differentiation from other movement disorders
- Improved long-term management and prognosis assessment
Understanding Your Genetic Test Results
Our comprehensive genetic counseling team will help interpret your results:
- Positive Result: Confirms SLC30A10 gene mutation and provides specific variant information for targeted management
- Negative Result: Rules out SLC30A10-related disorders, directing further diagnostic evaluation
- Variant of Uncertain Significance: Identifies genetic changes requiring additional clinical correlation
- Carrier Status: Determines inheritance patterns for family planning considerations
Test Pricing and Availability
| Test Feature | Details |
|---|---|
| Test Name | SLC30A10 Gene Hypermanganesemia with Dystonia Polycythemia and Cirrhosis NGS Genetic DNA Test |
| Discount Price | $500 USD |
| Regular Price | $700 USD |
| Turnaround Time | 3 to 4 Weeks |
| Sample Type | Blood, Extracted DNA, or One Drop Blood on FTA Card |
Nationwide Testing Availability
GGC DNA maintains comprehensive testing facilities across the United States, with convenient locations in major metropolitan areas including New York City, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our nationwide network ensures accessible genetic testing services for patients throughout the country.
Pre-Test Preparation Requirements
To ensure optimal testing accuracy, we require:
- Complete clinical history documentation
- Genetic counseling session for pedigree analysis
- Family history assessment for affected relatives
- Informed consent for genetic testing procedures
Take Control of Your Genetic Health Today
Don’t let uncertainty about neurological or metabolic symptoms delay your diagnosis. Our advanced NGS technology provides the clarity needed for proper management of SLC30A10-related disorders. Contact our genetic specialists to schedule your comprehensive evaluation and begin your journey toward definitive answers.
Call or WhatsApp our genetic counseling team today at +1(267) 388-9828 to book your SLC30A10 genetic test and take the first step toward understanding your genetic health.
