PEX10 Gene Zellweger Syndrome NGS Genetic DNA Test
Comprehensive Genetic Testing for Neurological Disorders
The PEX10 Gene Zellweger Syndrome NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for rare neurological conditions. This advanced test specifically targets mutations in the PEX10 gene, which plays a critical role in peroxisome biogenesis and function. Peroxisomes are essential cellular organelles responsible for various metabolic processes, and their dysfunction leads to Zellweger syndrome spectrum disorders.
What Does This Test Measure?
This comprehensive genetic analysis utilizes next-generation sequencing (NGS) technology to detect:
- Pathogenic variants in the PEX10 gene associated with Zellweger syndrome
- Single nucleotide polymorphisms (SNPs) affecting peroxisomal function
- Insertions, deletions, and copy number variations in the PEX10 locus
- Genetic markers linked to peroxisome biogenesis disorders
Who Should Consider This Test?
This genetic screening is recommended for individuals presenting with:
- Unexplained developmental delays in infancy
- Vision abnormalities including retinal degeneration
- Hearing impairment or sensorineural hearing loss
- Liver dysfunction and abnormal liver enzyme levels
- Hypotonia (reduced muscle tone) in newborns
- Seizures or neurological abnormalities
- Family history of peroxisomal disorders
- Consanguineous parentage with neurological concerns
Clinical Benefits of PEX10 Genetic Testing
Early detection through this comprehensive DNA analysis provides numerous advantages:
- Accurate diagnosis enabling targeted treatment approaches
- Improved disease management and symptom monitoring
- Informed family planning and genetic counseling
- Early intervention strategies for better outcomes
- Reduced diagnostic uncertainty and medical costs
- Personalized care plans based on genetic findings
Understanding Your Test Results
Our genetic specialists provide comprehensive interpretation of your results:
- Positive Result: Indicates presence of PEX10 gene mutation; requires consultation with neurologist and genetic counselor
- Negative Result: No detected mutations in PEX10 gene; other genetic causes may need investigation
- Variant of Uncertain Significance: Requires additional family studies and clinical correlation
- Carrier Status: Important for reproductive planning and family risk assessment
Test Information and Pricing
| Test Parameter | Details |
|---|---|
| Test Name | PEX10 Gene Zellweger Syndrome 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 |
| Specialty | Neurology |
| Department | Genetics |
| Method | NGS Technology |
| Disease Type | Neurological Disorders |
Pre-Test Requirements
Before scheduling your test, please ensure:
- Complete clinical history documentation
- Genetic counseling session to create family pedigree chart
- Discussion of testing implications with healthcare provider
- Understanding of potential outcomes and next steps
Nationwide Testing Availability
GGC DNA provides comprehensive genetic testing services across the United States. We have conveniently located branches in all major metropolitan areas including:
- New York City and surrounding regions
- Los Angeles and Southern California
- Chicago and Midwest locations
- Houston and Texas facilities
- Miami and Florida centers
- Seattle and Pacific Northwest clinics
Take Action Today
Don’t let uncertainty about neurological symptoms affect your quality of life. Our advanced PEX10 genetic testing provides the clarity needed for informed medical decisions. Contact our genetic specialists today to schedule your comprehensive evaluation.
Call or WhatsApp: +1(267) 388-9828
Book your PEX10 Gene Zellweger Syndrome NGS Genetic DNA Test today and take the first step toward understanding your genetic health. Our team of certified genetic counselors and neurologists are ready to provide the support and guidance you need throughout the testing process.
