PGAP1 Gene Mental Retardation Autosomal Recessive Type 42 NGS Genetic DNA Test
Comprehensive Genetic Testing for Intellectual Disability
The PGAP1 Gene Mental Retardation Autosomal Recessive Type 42 NGS Genetic DNA Test represents a breakthrough in neurological genetic diagnostics. This advanced test specifically targets mutations in the PGAP1 gene, which plays a critical role in brain development and cognitive function. When this gene malfunctions due to inherited mutations, it can lead to autosomal recessive mental retardation type 42, a condition characterized by significant intellectual disability and developmental challenges.
What Does This Test Measure?
Our NGS-based genetic test provides comprehensive analysis of the PGAP1 gene to identify pathogenic variants responsible for autosomal recessive mental retardation type 42. The test examines:
- Complete PGAP1 gene sequencing using Next-Generation Sequencing technology
- Detection of single nucleotide variants (SNVs) and small insertions/deletions
- Identification of compound heterozygous mutations
- Assessment of gene copy number variations when indicated
- Comprehensive variant interpretation by board-certified geneticists
Who Should Consider This Test?
This genetic test is recommended for individuals presenting with:
- Unexplained intellectual disability or developmental delay
- Family history of autosomal recessive inheritance patterns
- Consanguineous parentage with neurological symptoms
- Developmental regression in early childhood
- Multiple family members affected by similar cognitive impairments
- Unexplained seizures or movement disorders
- Speech and language development delays
Clinical Benefits of PGAP1 Genetic Testing
Undergoing PGAP1 genetic testing provides numerous advantages for patients and families:
- Accurate Diagnosis: Provides definitive identification of the genetic cause of intellectual disability
- Family Planning: Enables informed reproductive decisions and genetic counseling
- Treatment Guidance: Helps healthcare providers develop targeted intervention strategies
- Prognostic Information: Offers insights into disease progression and potential complications
- Early Intervention: Facilitates timely implementation of educational and therapeutic support
- Genetic Counseling: Provides comprehensive risk assessment for family members
Understanding Your Test Results
Your PGAP1 genetic test results will be carefully interpreted and explained during your genetic counseling session. Possible outcomes include:
- Positive Result: Identifies pathogenic mutations in both copies of the PGAP1 gene, confirming autosomal recessive mental retardation type 42 diagnosis
- Carrier Status: Detection of a single mutation indicating carrier status without disease manifestation
- Negative Result: No pathogenic mutations detected, suggesting other genetic or environmental causes
- Variant of Uncertain Significance: Identifies genetic changes with unclear clinical implications requiring further evaluation
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We have comprehensive testing facilities across the United States, with branches in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, San Francisco, and many more. Our state-of-the-art laboratories ensure consistent, high-quality results regardless of your location.
Take the Next Step Toward Genetic Clarity
If you or a family member are experiencing symptoms of intellectual disability or have concerns about genetic inheritance patterns, our PGAP1 Gene Mental Retardation Test provides the answers you need. Our team of genetic counselors and neurologists are ready to support you through every step of the testing process.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your PGAP1 genetic test. Take control of your genetic health with confidence and clarity.
