CentoIEM NGS Genetic DNA Test: Comprehensive Genetic Screening for Inherited Metabolic Disorders
Understanding the CentoIEM NGS Genetic DNA Test
The CentoIEM NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for neurological disorders. This comprehensive panel utilizes next-generation sequencing (NGS) technology to analyze over 150 genes associated with inherited metabolic diseases that primarily affect neurological function. These conditions, known as inborn errors of metabolism (IEM), can cause significant neurological impairment when left undiagnosed or untreated.
Early detection through the CentoIEM test is crucial because many metabolic disorders are treatable when identified promptly. The test provides healthcare providers with detailed genetic information that can guide treatment decisions, dietary modifications, and therapeutic interventions to prevent or minimize neurological damage.
What the CentoIEM Test Measures and Detects
The CentoIEM NGS Genetic DNA Test screens for a comprehensive range of inherited metabolic conditions including:
- Amino acid disorders (phenylketonuria, maple syrup urine disease)
- Organic acidemias (methylmalonic acidemia, propionic acidemia)
- Urea cycle disorders (ornithine transcarbamylase deficiency)
- Fatty acid oxidation disorders (medium-chain acyl-CoA dehydrogenase deficiency)
- Mitochondrial disorders affecting energy metabolism
- Peroxisomal disorders (adrenoleukodystrophy)
- Lysosomal storage diseases with neurological manifestations
- Neurotransmitter and cofactor metabolism disorders
Who Should Consider the CentoIEM Test
This advanced genetic test is recommended for individuals experiencing:
- Unexplained developmental delays or regression in children
- Recurrent seizures or epilepsy of unknown origin
- Movement disorders including ataxia, dystonia, or spasticity
- Metabolic crises with vomiting, lethargy, or coma
- Progressive neurological deterioration
- Family history of inherited metabolic disorders
- Abnormal newborn screening results requiring follow-up
- Unexplained intellectual disability or learning difficulties
- Metabolic acidosis or hyperammonemia of unknown cause
Benefits of Taking the CentoIEM Test
Choosing the CentoIEM NGS Genetic DNA Test offers numerous advantages:
- Comprehensive Analysis: Single test covering 150+ genes associated with metabolic neurological disorders
- Early Intervention: Enables timely treatment before irreversible neurological damage occurs
- Personalized Treatment: Results guide specific dietary, medication, and therapeutic interventions
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Cost-Effective: Replaces multiple individual genetic tests with one comprehensive panel
- Advanced Technology: Utilizes cutting-edge NGS for highest detection accuracy
- Expert Interpretation: Results reviewed by board-certified genetic specialists
Understanding Your Test Results
Your CentoIEM NGS Genetic DNA Test results will be carefully interpreted by our team of genetic specialists. The report will indicate:
- Positive Result: Identifies specific genetic mutations associated with metabolic disorders. This enables targeted treatment and management strategies.
- Negative Result: No disease-causing variants detected in the genes analyzed, though does not completely rule out all metabolic disorders.
- Variants of Uncertain Significance (VUS): Genetic changes with unclear clinical significance that may require additional family testing.
- Carrier Status: Identification of individuals carrying one copy of a mutation for recessive conditions.
All positive results include detailed clinical correlations, treatment recommendations, and referral to appropriate metabolic specialists. Genetic counseling is strongly recommended to fully understand the implications of your results.
Test Pricing and Availability
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $750 |
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood, Extracted DNA, or One Drop Blood on FTA Card
- Methodology: Next-Generation Sequencing (NGS) Technology
- Specialty: Neurology and Genetics
Pre-Test Requirements
Before taking the CentoIEM NGS Genetic DNA Test, patients should provide:
- Complete clinical history of neurological symptoms
- Genetic counseling session to create detailed family pedigree
- Documentation of affected family members when available
Nationwide Availability
GGC DNA has testing facilities conveniently located throughout the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network of certified collection centers ensures accessible testing for patients across the country.
Book Your CentoIEM Test Today
Take the first step toward understanding your neurological health with the comprehensive CentoIEM NGS Genetic DNA Test. Our experienced genetic counselors and neurological specialists are ready to guide you through the testing process and help interpret your results.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your appointment or learn more about how the CentoIEM test can provide crucial insights into inherited metabolic disorders affecting neurological function.
Early detection through advanced genetic testing can make a significant difference in managing metabolic neurological conditions. Contact GGC DNA now to book your CentoIEM NGS Genetic DNA Test and take control of your neurological health.
