CLMP Gene Congenital Short Bowel Syndrome NGS Genetic DNA Test
Comprehensive Genetic Analysis for Pediatric Intestinal Disorders
The CLMP Gene Congenital Short Bowel Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations responsible for congenital short bowel syndrome (CSBS). This rare but serious condition affects infants and children, causing significant intestinal malabsorption and nutritional challenges. Our advanced genetic testing provides families and healthcare providers with definitive answers about this complex disorder.
What Does This Test Measure and Detect?
This specialized genetic test utilizes next-generation sequencing (NGS) technology to comprehensively analyze the CLMP (coxsackie and adenovirus receptor-like membrane protein) gene. The test specifically identifies:
- Pathogenic variants in the CLMP gene associated with congenital short bowel syndrome
- Single nucleotide polymorphisms (SNPs) affecting protein function
- Insertion and deletion mutations impacting intestinal development
- Genetic markers for autosomal recessive inheritance patterns
- Variants affecting intestinal epithelial cell adhesion and organization
Who Should Consider This Genetic Test?
This test is particularly recommended for individuals presenting with the following symptoms or clinical scenarios:
- Infants with persistent diarrhea and failure to thrive despite adequate nutrition
- Children with documented short bowel length on imaging studies
- Patients requiring prolonged parenteral nutrition support
- Individuals with family history of congenital intestinal disorders
- Suspected cases of intestinal malrotation or atresia
- Unexplained nutritional deficiencies and growth retardation
- Recurrent abdominal distension and feeding intolerance
Significant Benefits of Genetic Testing
Undergoing the CLMP gene test provides numerous advantages for patients and families:
- Accurate Diagnosis: Confirms or rules out genetic causes of short bowel syndrome
- Personalized Treatment: Enables targeted nutritional and medical management strategies
- Family Planning: Provides crucial information for genetic counseling and reproductive decisions
- Early Intervention: Facilitates timely implementation of specialized care protocols
- Prognostic Information: Helps predict disease progression and long-term outcomes
- Research Contribution: Advances understanding of rare genetic intestinal disorders
Understanding Your Test Results
Our comprehensive genetic report provides clear interpretation of your results with clinical context:
- Positive Result: Indicates the presence of pathogenic CLMP gene mutations consistent with congenital short bowel syndrome diagnosis
- Negative Result: Suggests that CLMP gene mutations are not detected, though other genetic or non-genetic causes should be considered
- Variant of Uncertain Significance: Identifies genetic changes whose clinical significance requires further investigation
- 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 consultation with genetic specialists and pediatric gastroenterologists.
Test Pricing and Availability
| 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, and San Jose. Our network of certified genetic testing facilities ensures consistent quality and reliable results nationwide.
Take Action for Your Genetic Health
Don’t let uncertainty about congenital short bowel syndrome affect your family’s wellbeing. Our specialized genetic testing provides the clarity needed for informed medical decisions and comprehensive care planning. Contact our genetic counseling team today to schedule your test and begin your journey toward definitive answers.
Call or WhatsApp: +1(267) 388-9828 to book your CLMP Gene Congenital Short Bowel Syndrome NGS Genetic DNA Test today. Our compassionate genetic specialists are ready to guide you through the testing process and provide the support your family deserves.
