SARDH Gene Sarcosinemia NGS Genetic DNA Test
Comprehensive Genetic Testing for Metabolic Disorders
The SARDH Gene Sarcosinemia NGS Genetic DNA Test represents a breakthrough in metabolic disorder diagnostics, offering precise detection of genetic mutations associated with sarcosinemia. This rare inherited condition affects the body’s ability to properly metabolize sarcosine, leading to potential neurological complications and developmental challenges. Our advanced testing methodology provides healthcare providers with critical information for accurate diagnosis and personalized treatment planning.
What This Test Measures and Detects
This sophisticated genetic analysis specifically targets the SARDH (sarcosine dehydrogenase) gene, which plays a crucial role in the glycine cleavage system. The test identifies:
- Pathogenic variants and mutations in the SARDH gene
- Single nucleotide polymorphisms affecting enzyme function
- Deletions, insertions, and copy number variations
- Compound heterozygous and homozygous mutations
- Novel genetic variants with potential clinical significance
Who Should Consider This Test
This genetic screening is particularly recommended for individuals presenting with:
- Unexplained neurological symptoms including seizures or tremors
- Developmental delays in infancy or childhood
- Family history of metabolic disorders or sarcosinemia
- Elevated sarcosine levels in blood or urine tests
- Progressive neurological deterioration without clear cause
- Consanguineous parentage with metabolic concerns
Clinical Benefits of Genetic Testing
Undergoing the SARDH Gene Sarcosinemia NGS Genetic DNA Test provides numerous advantages:
- Accurate Diagnosis: Confirms or rules out sarcosinemia with high precision
- Early Intervention: Enables proactive management before severe symptoms develop
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Personalized Treatment: Guides dietary modifications and therapeutic approaches
- Prognostic Information: Helps predict disease progression and potential complications
- Peace of Mind: Reduces diagnostic uncertainty for patients and families
Understanding Your Test Results
Our comprehensive genetic report includes detailed interpretation of your results:
- Positive Result: Indicates presence of pathogenic SARDH gene mutations confirming sarcosinemia diagnosis
- Negative Result: Suggests absence of known disease-causing variants in the SARDH gene
- Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
- Carrier Status: Detects individuals carrying one copy of mutated gene without disease symptoms
All results are accompanied by detailed clinical guidance and recommendations for next steps in management.
Test Pricing Information
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
Nationwide Testing Availability
We proudly serve patients across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified genetic counselors and medical professionals ensures consistent, high-quality care regardless of location.
Take Control of Your Genetic Health Today
Don’t let uncertainty about metabolic disorders affect your quality of life. Our SARDH Gene Sarcosinemia NGS Genetic DNA Test provides the clarity you need for informed healthcare decisions. With results available in 3-4 weeks and simple sample collection (blood, extracted DNA, or one drop of blood on FTA card), getting tested has never been more convenient.
Call +1(267) 388-9828 now to schedule your genetic counseling session and book your test. Our dedicated team is ready to assist you with comprehensive pre-test guidance and post-test support.
