Test Price
2,800 AED✅ Home Collection Available
CLMP Gene Congenital Short-Bowel Syndrome Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين CLMP لمتلازمة الأمعاء القصيرة الخلقية في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary & Patient Guarantee
Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited NGS Processing (Cert: INT/EGQ/2509DA/3139).
ضمان الدقة: حساسية تشخيصية 99.9% عبر معالجة تسلسل الجيل التالي المعتمدة من ISO.
Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM).
Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation with a genetic counsellor.
Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731. All UAE payers accepted.
Regulatory Compliance & Data Sovereignty
This laboratory service strictly follows Federal Decree-Law No. 41 of 2024 (Art. 87) on Patient Health Data, Child Data Sovereignty (CDS) Law 2026 (minors), and UAE PDPL. All genetic information is stored and processed locally within the UAE. ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139).
Overview
This targeted Next-Generation Sequencing (NGS) analysis examines the entire coding region of the CLMP gene to detect pathogenic variants responsible for congenital short-bowel syndrome, a severe neonatal dysmorphology disorder. يقوم هذا الاختبار الجيني بتحليل كامل المنطقة المشفرة لجين CLMP لتشخيص متلازمة الأمعاء القصيرة الخلقية، وهو اضطراب شديد يصيب حديثي الولادة.
| Feature | Our CLMP NGS Test | Closest Alternative (WES/Generic Panel) |
|---|---|---|
| Diagnostic Precision | 99.9% sensitivity; full gene coverage with >200x depth | May have incomplete CLMP coverage or lower depth; risk of false negatives |
| Methodology | Targeted NGS + Sanger confirmation | Whole-exome sequencing with incidental findings; unfocused |
| Turnaround Time | 3–4 weeks | Often 6–10 weeks plus additional validation |
| Clinical Relevance | Specific report for short-bowel syndrome, including ACMG classification | May miss or misinterpret rare CLMP variants due to limited focus |
Physician Insight & Safety Protocol
"As a clinical geneticist, I understand the profound anxiety families experience when congenital short-bowel syndrome is suspected. This CLMP test provides definitive molecular answers, but it must be correlated with full clinical, surgical, and nutritional assessments. Never alter management based on a genetic result alone — always consult your pediatric gastroenterologist and geneticist first."
— Dr. PRABHAKAR REDDY, DHA License: 61713011
Do not discontinue prescribed medication or nutritional support without consulting your doctor.
Safety Alert – Exclusion Criteria & Emergency Red Flags
- Exclusion: This test is not indicated for asymptomatic individuals without a clinical suspicion of short-bowel syndrome. Samples collected on FTA cards must meet quality standards; hemolyzed, clotted, or insufficient specimens will be rejected.
- Exclusion: Patients experiencing acute, life-threatening gastrointestinal emergencies (e.g., massive bowel infarction, toxic megacolon) should prioritise emergency surgical intervention over elective genetic testing.
- ER Red Flag: If your child develops sudden severe dehydration, electrolyte imbalances, intractable vomiting, or bowel obstruction symptoms during the testing window, seek immediate medical attention at the nearest emergency department.
Patient FAQ & Clinical Guidance
What is the CLMP gene and how does it relate to congenital short-bowel syndrome?
The CLMP gene encodes a transmembrane protein essential for intestinal development; pathogenic variants cause congenital short-bowel syndrome with severe malabsorption, failure to thrive, and dependence on parenteral nutrition. يُشفّر جين CLMP بروتينًا غشائيًا أساسيًا لنمو الأمعاء؛ وتسبب الطفرات المَرَضية متلازمة الأمعاء القصيرة الخلقية مع سوء امتصاص حاد وفشل في النمو واعتماد على التغذية الوريدية.
What sample types are accepted and how does the home collection work?
We accept whole blood (EDTA), extracted DNA, or a single drop of blood on an FTA card; our ISO-certified cold-chain phlebotomy team will collect your child’s sample at home between 8 AM and 11 PM, ensuring stability and rapid transport. نقبل الدم الكامل (EDTA) أو الحمض النووي المستخلص أو قطرة دم واحدة على بطاقة FTA؛ وسيقوم فريق الفصد المنزلي المعتمد بجمع عينة طفلك بين الثامنة صباحًا والحادية عشرة مساءً مع ضمان الاستقرار والنقل السريع.
How long does it take to receive results and who will explain them?
The laboratory delivers a comprehensive clinical report within 3 to 4 weeks; you will receive a post- telephonic consultation with a genetic counsellor to interpret the findings and discuss next steps for your child’s care. يُصدر المختبر تقريرًا سريريًا شاملًا خلال 3 إلى 4 أسابيع؛ وستتلقى استشارة هاتفية بعد الاختبار مع مستشار وراثي لتفسير النتائج ومناقشة الخطوات التالية لرعاية طفلك.
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التحقق من التغطية التأمينية
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Stop the guesswork. Send a photo of your Insurance Card and Doctor's Prescription to our DHA-Certified Verification Team on WhatsApp.
توقف عن التخمين. أرسل صورة من بطاقة التأمين ووصفة الطبيب إلى فريق التحقق المعتمد من هيئة الصحة بدبي عبر الواتساب. احصل على تحديث الحالة في دقائق.
Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians