NEUROG3 Gene Diarrhea Type 4 Malabsorptive Congenital NGS Genetic DNA Test
Comprehensive Genetic Testing for Congenital Diarrhea Disorders
The NEUROG3 Gene Diarrhea Type 4 Malabsorptive Congenital NGS Genetic DNA Test represents a breakthrough in pediatric gastroenterology diagnostics. This advanced genetic test specifically targets mutations in the NEUROG3 gene, which plays a critical role in intestinal endocrine cell development and function. When this gene malfunctions, it leads to severe congenital diarrhea type 4, a rare but devastating metabolic disorder affecting infants from birth.
What Does This Test Measure?
Our comprehensive NGS genetic analysis detects specific mutations and variations in the NEUROG3 gene that are responsible for:
- Complete sequencing of the NEUROG3 gene coding regions
- Detection of point mutations, insertions, and deletions
- Identification of splice site variants affecting gene function
- Assessment of autosomal recessive inheritance patterns
- Evaluation of genetic markers associated with intestinal malabsorption
Who Should Consider This Test?
This specialized genetic test is recommended for individuals presenting with:
- Infants with persistent, watery diarrhea beginning in the first weeks of life
- Children experiencing failure to thrive despite adequate nutrition
- Patients with severe malabsorption and nutritional deficiencies
- Individuals with family history of congenital diarrhea disorders
- Cases where standard diarrhea treatments have proven ineffective
- Suspected metabolic disorders affecting intestinal function
Clinical Benefits of NEUROG3 Genetic Testing
Early genetic diagnosis through our NEUROG3 test provides numerous clinical advantages:
- Accurate Diagnosis: Confirms congenital diarrhea type 4 with genetic certainty
- Personalized Treatment: Enables targeted nutritional and medical interventions
- Family Planning: Provides recurrence risk information for future pregnancies
- Prognostic Information: Helps predict disease progression and complications
- Therapeutic Guidance: Informs appropriate management strategies
- Genetic Counseling: Supports families in understanding inheritance patterns
Understanding Your Test Results
Our comprehensive genetic report provides clear, actionable information:
- Positive Result: Confirms NEUROG3 gene mutation and diagnosis of congenital diarrhea type 4
- Negative Result: Rules out NEUROG3-related diarrhea, suggesting alternative causes
- Variant of Uncertain Significance: Identifies genetic changes requiring further investigation
- Carrier Status: Determines if individuals carry one copy of the mutated gene
All results include detailed interpretation by our board-certified genetic specialists, with recommendations for clinical management and follow-up care.
Test Pricing and Availability
| Test Component | Price (USD) |
|---|---|
| Discount Price | $500 |
| Regular Price | $700 |
| Turnaround Time | 3-4 Weeks |
| Sample Type | Blood, Extracted DNA, or Blood on FTA Card |
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 collection centers ensures accessible genetic testing for families nationwide.
Take the Next Step Toward Diagnosis
If you or your child are experiencing symptoms of congenital diarrhea or have concerns about inherited metabolic disorders, our NEUROG3 genetic test provides the answers you need. Early diagnosis can significantly improve outcomes and quality of life for affected individuals.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic consultation and testing appointment. Our compassionate genetic counselors are available to discuss your concerns, explain the testing process, and help you understand how genetic testing can benefit your family.
Don’t let uncertainty about congenital diarrhea disorders delay proper diagnosis and treatment. Contact us now to begin your journey toward genetic clarity and personalized medical care.
