MAN1B1 Gene Mental Retardation Autosomal Recessive Type 15 NGS Genetic DNA Test
Comprehensive Genetic Testing for Intellectual Disability
The MAN1B1 Gene Mental Retardation Autosomal Recessive Type 15 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This advanced next-generation sequencing test specifically targets mutations in the MAN1B1 gene, which plays a critical role in protein glycosylation and neurological development. When this gene functions improperly, it can lead to autosomal recessive mental retardation type 15, a condition characterized by significant intellectual disability and developmental delays.
What This Test Measures and Detects
Our sophisticated NGS technology examines the entire MAN1B1 gene sequence to identify:
- Point mutations and single nucleotide variants
- Small insertions and deletions (indels)
- Copy number variations affecting the MAN1B1 gene
- Pathogenic variants associated with autosomal recessive inheritance
- Novel mutations that may not be documented in existing databases
Who Should Consider This Test
This genetic test is particularly recommended for individuals presenting with:
- Unexplained intellectual disability or developmental delays
- Family history of autosomal recessive neurological disorders
- Consanguineous parentage with neurological symptoms in offspring
- Multiple family members affected by similar cognitive impairments
- Children with delayed motor milestones and speech development
- Individuals with co-occurring neurological features without clear diagnosis
Key Benefits of MAN1B1 Genetic Testing
Undergoing this comprehensive genetic analysis provides numerous advantages:
- Accurate Diagnosis: Confirms or rules out MAN1B1-related mental retardation
- Family Planning Guidance: Enables informed reproductive decisions
- Early Intervention: Facilitates timely educational and therapeutic support
- Genetic Counseling: Provides basis for personalized genetic counseling sessions
- Research Contribution: Helps advance understanding of neurological genetic disorders
- Peace of Mind: Reduces diagnostic uncertainty for families
Understanding Your Test Results
Our comprehensive report includes detailed interpretation of your genetic findings:
- Positive Result: Indicates presence of pathogenic MAN1B1 mutations consistent with autosomal recessive mental retardation type 15
- Negative Result: Suggests absence of known disease-causing variants in the MAN1B1 gene
- Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications requiring further evaluation
- Carrier Status: Determines if individuals carry one copy of a mutated gene without showing symptoms
All results are accompanied by detailed explanations and recommendations for next steps, including referral to appropriate specialists and genetic counselors.
Test Pricing Information
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
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 support throughout the testing process.
Take the Next Step Toward Genetic Clarity
Don’t let uncertainty about neurological conditions affect your family’s future. Our MAN1B1 Gene Mental Retardation Test provides the answers you need for informed healthcare decisions. With results typically available within 3-4 weeks and multiple sample collection options including blood, extracted DNA, or blood spots on FTA cards, getting tested has never been more convenient.
Ready to schedule your test? Call our genetic specialists today at +1(267) 388-9828 or book your appointment online. Take control of your genetic health with confidence and clarity.
