GAD1 Gene Cerebral Palsy Type 1 Spastic Quadriplegic NGS Genetic DNA Test
Comprehensive Genetic Analysis for Cerebral Palsy Diagnosis
The GAD1 Gene Cerebral Palsy Type 1 Spastic Quadriplegic NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This advanced test specifically targets mutations in the GAD1 (glutamate decarboxylase 1) gene, which plays a critical role in the production of GABA (gamma-aminobutyric acid), the primary inhibitory neurotransmitter in the central nervous system. When GAD1 gene mutations occur, they can disrupt normal brain development and function, leading to cerebral palsy type 1 with spastic quadriplegic presentation.
What This Test Measures and Detects
Our sophisticated NGS (Next-Generation Sequencing) technology enables comprehensive analysis of the GAD1 gene to identify:
- Point mutations and single nucleotide variations
- Insertions and deletions in the genetic sequence
- Copy number variations affecting gene function
- Pathogenic variants associated with cerebral palsy type 1
- Inheritance patterns and familial risk assessment
The test provides detailed information about specific genetic alterations that impair GABA synthesis, leading to the neurological symptoms characteristic of spastic quadriplegic cerebral palsy.
Who Should Consider This Test
This genetic test is recommended for individuals presenting with:
- Early-onset spasticity affecting all four limbs
- Developmental delays in motor milestones
- Muscle stiffness and hypertonia
- Difficulty with coordination and movement
- Family history of cerebral palsy or neurological disorders
- Unexplained neurological symptoms in infancy or childhood
- Suspected genetic basis for cerebral palsy symptoms
Key Benefits of GAD1 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages:
- Accurate Diagnosis: Confirms the genetic basis of cerebral palsy symptoms
- Personalized Treatment: Enables targeted therapeutic interventions
- Family Planning: Provides crucial information for genetic counseling
- Prognostic Information: Helps predict disease progression and outcomes
- Early Intervention: Facilitates timely management strategies
- Research Contribution: Advances understanding of neurological genetics
Understanding Your Test Results
Our comprehensive genetic counseling service helps you interpret your results:
- Positive Result: Indicates the presence of GAD1 gene mutations associated with cerebral palsy type 1
- Negative Result: Suggests that GAD1 mutations are not the cause of symptoms
- Variant of Uncertain Significance: Requires further clinical correlation
- Carrier Status: Identifies individuals who may pass mutations to offspring
Our genetic counselors provide detailed explanations of inheritance patterns, recurrence risks, and management recommendations based on your specific results.
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
Pre-test Requirements: Clinical History and Genetic Counseling Session
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network of certified genetic counselors and neurological specialists ensures you receive comprehensive care and support throughout the testing process.
Take the Next Step Toward Clarity
If you or your loved one is experiencing symptoms of cerebral palsy or has a family history of neurological disorders, don’t wait to get answers. Our GAD1 Gene Cerebral Palsy Type 1 Spastic Quadriplegic NGS Genetic DNA Test provides the clarity needed for informed medical decisions and personalized care planning.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our compassionate team is ready to guide you through every step of the process and help you understand your genetic health.
