Spinocerebellar Ataxia SCA Panel 1, 2, 3, 6, 7, 10, 12 Genetic Test
Comprehensive Genetic Testing for Hereditary Ataxia Disorders
The Spinocerebellar Ataxia (SCA) Panel represents a cutting-edge genetic diagnostic tool designed to identify specific hereditary ataxia conditions affecting the cerebellum and spinal cord. This comprehensive panel analyzes seven of the most common SCA subtypes that collectively account for a significant portion of hereditary ataxia cases worldwide. Early and accurate genetic diagnosis is crucial for proper disease management, treatment planning, and genetic counseling.
What This Advanced Genetic Test Detects
Our SCA Panel utilizes sophisticated End Point PCR technology to detect abnormal CAG trinucleotide repeat expansions in specific genes associated with spinocerebellar ataxia:
- SCA1: ATXN1 gene mutations causing progressive cerebellar degeneration
- SCA2: ATXN2 gene abnormalities leading to widespread neurological symptoms
- SCA3 (Machado-Joseph Disease): ATXN3 gene defects resulting in complex movement disorders
- SCA6: CACNA1A gene mutations primarily affecting coordination
- SCA7: ATXN7 gene expansions often accompanied by vision problems
- SCA10: ATXN10 gene abnormalities with potential seizure manifestations
- SCA12: PPP2R2B gene mutations causing tremor-predominant symptoms
Who Should Consider This Genetic Test?
This comprehensive SCA panel is recommended for individuals experiencing:
- Progressive difficulty with balance and coordination
- Unsteady gait and frequent stumbling
- Slurred speech or changes in speech patterns
- Involuntary eye movements (nystagmus)
- Family history of similar neurological symptoms
- Unexplained tremors or muscle stiffness
- Difficulty with fine motor tasks like writing or buttoning clothes
- Progressive vision problems in combination with movement issues
Clinical Indications and Symptoms
Patients typically present with symptoms that gradually worsen over time, including:
- Progressive ataxia affecting walking and coordination
- Dysarthria (slurred or slow speech)
- Oculomotor abnormalities and visual disturbances
- Peripheral neuropathy in some subtypes
- Cognitive changes and executive function impairment
- Swallowing difficulties in advanced stages
Significant Benefits of SCA Genetic Testing
Undergoing the Spinocerebellar Ataxia Panel provides numerous advantages for patients and their families:
- Accurate Diagnosis: Confirms specific SCA subtype for targeted management
- Early Intervention: Enables proactive treatment and symptom management
- Genetic Counseling: Provides essential information for family planning decisions
- Prognostic Information: Helps understand disease progression patterns
- Clinical Trial Eligibility: Opens opportunities for emerging treatments
- Family Screening: Identifies at-risk relatives for preventive monitoring
- Peace of Mind: Reduces diagnostic uncertainty and anxiety
Understanding Your Test Results
Our genetic specialists provide comprehensive interpretation of your SCA panel results:
- Normal Results: No abnormal CAG repeat expansions detected in tested genes
- Intermediate Alleles: Repeat numbers between normal and disease range may require monitoring
- Expanded Alleles: CAG repeats exceeding normal range confirm SCA diagnosis
- Specific Subtype Identification: Precise genetic mutation identified for targeted care
All positive results include detailed genetic counseling to help you understand implications, inheritance patterns, and next steps for management and family planning.
Test Information and Pricing
| Test Component | Details |
|---|---|
| Test Name | Spinocerebellar Ataxia SCA Panel 1, 2, 3, 6, 7, 10, 12 |
| Regular Price | $500 USD |
| Discount Price | $376 USD |
| Turnaround Time | 5-7 days |
| Sample Type | Peripheral Blood |
| Test Components | EDTA Vacutainer (2ml) |
| Testing Method | End Point PCR |
Pre-Test Instructions
The Spinocerebellar Ataxia (SCA Panel – 1, 2, 3, 6, 7, 10 & 12) requires a Doctor’s prescription. Please note that prescription requirements do not apply for surgery and pregnancy cases or individuals planning to travel abroad.
Nationwide Testing Availability
We have diagnostic centers conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, Charlotte, San Francisco, Indianapolis, Seattle, Denver, Washington DC, Boston, El Paso, Nashville, Detroit, Oklahoma City, Portland, Las Vegas, Memphis, Louisville, Baltimore, and Milwaukee.
Take Control of Your Neurological Health Today
Don’t let uncertainty about hereditary ataxia conditions affect your quality of life. Our comprehensive SCA Panel provides the clarity you need for informed healthcare decisions. With rapid 5-7 day turnaround and expert genetic counseling support, you’ll receive the answers you deserve.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your Spinocerebellar Ataxia genetic testing appointment. Our genetic specialists are ready to answer your questions and help you take the next step toward understanding your neurological health.
Early genetic diagnosis can make a significant difference in managing spinocerebellar ataxia symptoms and planning for the future. Contact us now to book your $376 USD SCA Panel test and gain the genetic insights that matter for you and your family.
