Sale!

CLMP Gene Congenital Short-Bowel Syndrome NGS Genetic DNA Test

Original price was: R9,350.Current price is: R6,700.

-28%

Facing concerns about your child’s digestive health? Our CLMP Gene Congenital Short-Bowel Syndrome NGS Genetic DNA Test provides definitive answers for families across South Africa. For only ZAR 6,700 (regularly ZAR 9,350), this advanced genetic test uses Next Generation Sequencing technology to detect mutations in the CLMP gene that cause congenital short-bowel syndrome. Early detection through our accurate testing can guide proper nutritional management and treatment planning, potentially preventing life-threatening complications. We understand the anxiety parents feel when their child struggles with feeding difficulties and poor growth – that’s why we offer comprehensive genetic counselling alongside testing. Our trusted laboratory delivers results within 3-4 weeks, giving you the clarity needed to make informed healthcare decisions for your child’s future.

📞 24/7 South African Support Team Call : +27 6412 56421

  • ✓ ISO Accredited Lab Reports
  • ✓ Free Genetic Counseling Included
  • 🔒 100% Confidential & Secure Testing
Guaranteed Safe Checkout

CLMP Gene Short-Bowel Syndrome Test | ZAR 6
CLMP Gene Congenital Short-Bowel Syndrome NGS Genetic DNA Test
R9,350 Original price was: R9,350.R6,700Current price is: R6,700.

[wpforms id=”1190″ title=”true” description=”Request a call back”]

Understanding Your Child’s Digestive Health Concerns

As a parent, watching your child struggle with feeding difficulties, poor weight gain, or digestive issues can be incredibly worrying. When conventional treatments don’t provide answers, genetic testing for congenital short-bowel syndrome offers hope and clarity. At Oracle Genomics, we understand the emotional journey families face and provide compassionate, accurate genetic testing to help you understand your child’s health challenges.

What Does This Test Detect?

Our CLMP Gene Congenital Short-Bowel Syndrome NGS Genetic DNA Test specifically analyses the CLMP gene using advanced Next Generation Sequencing technology. This gene plays a crucial role in intestinal development, and mutations can lead to congenital short-bowel syndrome – a condition where infants are born with an abnormally short small intestine, causing severe nutritional absorption problems.

Who Should Consider This Test?

This test is particularly important for:

  • Infants experiencing persistent feeding difficulties and failure to thrive
  • Children with unexplained chronic diarrhoea and malnutrition
  • Babies requiring prolonged parenteral nutrition support
  • Families with a history of intestinal abnormalities or digestive disorders
  • Parents concerned about their child’s growth and development patterns

Why Early Detection Matters for Your Child’s Health

Early diagnosis through genetic testing provides numerous benefits:

  • Personalised Treatment Planning: Knowing the genetic cause allows for tailored nutritional and medical management
  • Prevention of Complications: Early intervention can prevent severe malnutrition and developmental delays
  • Family Planning Guidance: Understanding inheritance patterns helps with future family planning decisions
  • Peace of Mind: Eliminating uncertainty reduces parental stress and anxiety
  • Improved Quality of Life: Proper management leads to better growth and development outcomes

Understanding Your Test Results

We make understanding genetic results simple and reassuring. Our comprehensive report includes:

  • Clear explanation of CLMP gene findings in easy-to-understand language
  • Detailed interpretation of how results relate to your child’s symptoms
  • Personalised recommendations for medical management and nutritional support
  • Access to genetic counselling to discuss results and next steps
  • Ongoing support for implementing recommended care plans

Transparent Pricing and Value

Service Regular Price Special Price
CLMP Gene Test ZAR 9,350 ZAR 6,700
Genetic Counselling Session Included
Family Pedigree Analysis Included
Results Interpretation Included

Considering the potential lifetime costs of untreated congenital short-bowel syndrome complications, this test represents exceptional value for your child’s long-term health.

Nationwide Accessibility and Trust

Oracle Genomics brings advanced genetic testing to families across South Africa with convenient testing locations in Johannesburg, Cape Town, Durban, and Pretoria. Our NGS technology ensures 99.9% accuracy, and all testing is performed in our SANAS-accredited laboratory by experienced genetic specialists.

Take Action for Your Child’s Health Today

Don’t let uncertainty about your child’s digestive health continue. Early detection through genetic testing can make a significant difference in treatment outcomes and quality of life. Our compassionate team is ready to support you through every step of the testing process.

Book your consultation today and take the first step toward understanding your child’s genetic health. Call us at [INSERT PHONE] or visit our website to schedule your appointment. Remember – every day matters when it comes to your child’s development and wellbeing.