LCT Gene Lactase Deficiency Congenital NGS Genetic DNA Test
Comprehensive Genetic Analysis for Congenital Lactase Deficiency
The LCT Gene Lactase Deficiency Congenital NGS Genetic DNA Test represents a breakthrough in genetic diagnostics for metabolic disorders. This advanced testing methodology provides definitive identification of mutations in the LCT gene, which encodes the lactase enzyme essential for lactose digestion. Congenital lactase deficiency is a rare autosomal recessive disorder that manifests from birth, causing severe gastrointestinal distress and nutritional challenges in affected infants.
What This Test Measures and Detects
Our comprehensive NGS-based genetic test specifically targets and sequences the entire LCT gene to identify pathogenic variants responsible for congenital lactase deficiency. The test detects:
- Point mutations and single nucleotide variants in the LCT gene
- Insertions and deletions affecting lactase enzyme production
- Regulatory region mutations impacting gene expression
- Known pathogenic variants associated with congenital lactase deficiency
- Novel genetic variations requiring clinical correlation
Who Should Consider This Genetic Test
This specialized genetic screening is recommended for individuals presenting with:
- Infants experiencing severe diarrhea, vomiting, and dehydration after breastfeeding or formula feeding
- Failure to thrive in newborns despite adequate caloric intake
- Family history of congenital lactase deficiency or consanguineous parents
- Persistent gastrointestinal symptoms unresponsive to standard treatments
- Suspected metabolic disorders with lactose intolerance symptoms
- Unexplained nutritional deficiencies in early childhood
Significant Benefits of Genetic Testing
Undergoing the LCT Gene Lactase Deficiency Congenital NGS Genetic DNA Test provides numerous advantages:
- Definitive Diagnosis: Eliminates diagnostic uncertainty and enables targeted management
- Early Intervention: Facilitates immediate dietary modifications to prevent complications
- Family Planning: Provides crucial genetic information for future family planning decisions
- Personalized Treatment: Guides development of individualized nutritional strategies
- Prevention of Complications: Helps avoid severe dehydration, malnutrition, and developmental delays
- Genetic Counseling: Supports informed decision-making for affected families
Understanding Your Test Results
Our comprehensive genetic analysis provides clear, actionable results:
- Positive Result: Indicates presence of pathogenic LCT gene mutations confirming congenital lactase deficiency diagnosis
- Negative Result: Suggests absence of tested mutations, though clinical correlation remains essential
- Variant of Uncertain Significance: Identifies genetic changes requiring additional clinical evaluation
- Carrier Status: Determines if individuals carry one copy of mutated gene without disease manifestation
Test Pricing Information
| Test Component | Price (USD) |
|---|---|
| LCT Gene Lactase Deficiency Congenital NGS Genetic DNA Test – Discount Price | $500 |
| LCT Gene Lactase Deficiency Congenital NGS Genetic DNA Test – Regular Price | $700 |
Nationwide Testing Availability
General Genetics Corporation provides comprehensive genetic testing services across the United States. We have established branches in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and numerous other cities. Our nationwide network ensures accessible genetic testing for patients throughout the country.
Take Control of Your Genetic Health Today
Don’t let uncertainty about congenital lactase deficiency affect your quality of life or your child’s development. Our advanced NGS genetic testing provides the clarity needed for proper diagnosis and management. Contact our genetic specialists today to schedule your comprehensive LCT gene analysis.
Call or WhatsApp: +1(267) 388-9828 to book your genetic test consultation and take the first step toward definitive diagnosis and personalized treatment planning.
