Test Price
2,800 AED✅ Home Collection Available
WDR35 Gene (Cranioectodermal Dysplasia Type 2) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين WDR35 (خلل التنسج القحفي الظاهر النوع 2) بتقنية التسلسل الجيني المتقدم في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary & Guarantees (ملخص تنفيذي)
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Certified Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain, available 8 AM – 11 PM. خدمة سحب عينات منزلية معتمدة وفق معايير الآيزو.
- Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance to interpret your results with a genetic specialist.
- Insurance: Direct Billing Verification via WhatsApp at +971545488731.
Test Overview
The WDR35 Gene Genetic Test screens for pathogenic variants associated with Cranioectodermal Dysplasia Type 2 (CED2), a rare ciliopathy characterized by skeletal abnormalities, ectodermal defects, and renal involvement. This advanced Next-Generation Sequencing analysis offers definitive molecular diagnosis, guiding pediatric management and genetic counseling. (يكشف تحليل جين WDR35 عن الطفرات المسببة لخلل التنسج القحفي الظاهر النوع 2.)
Our Test vs. Closest Alternative
| Feature | Our WDR35 NGS Test | Targeted Variant Panel |
|---|---|---|
| Precision | Full gene sequencing & deletion/duplication analysis | Only known hotspots; may miss novel mutations |
| Methodology | Next-Generation Sequencing (NGS) with bioinformatic validation | Sanger sequencing or limited MLPA |
| Turnaround Time | 3–4 Weeks | 4–6 Weeks (often outsourced) |
Physician Insight & Safety Protocol
“Cranioectodermal dysplasia type 2 is a complex multisystem disorder where genotype-phenotype correlation is critical; this NGS test provides the molecular confirmation necessary to tailor surveillance and family planning. As a clinician, I strongly recommend that results be interpreted in the context of comprehensive clinical evaluation, never in isolation.”
— Dr. Prabhakar Reddy, DHA License: 61713011, Specialist Genetic Pediatrician
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor. This genetic test does not replace ongoing medical management.
Safety & Exclusion Criteria
- Sample Rejection: Grossly hemolyzed, clotted, or incorrectly stored whole blood samples will be rejected.
- Patient Exclusion: Individuals currently receiving heparin therapy (use alternative anticoagulant collection) or those who have undergone hematopoietic stem cell transplant within 90 days; results may be confounded.
- Emergency Red Flags: If you or your child experience acute renal colic, sudden vision loss, or severe respiratory distress, seek immediate emergency care — do not wait for test results. This test is not a substitute for urgent evaluation.
Patient FAQ & Clinical Guidance
1. What does the WDR35 genetic test detect and why is family history important?
The test identifies pathogenic variants in the WDR35 gene that cause cranioectodermal dysplasia type 2, a condition inherited in an autosomal recessive manner; therefore, a detailed pedigree helps assess carrier status and recurrence risk for future pregnancies. يكشف التحليل عن الطفرات المرضية في جين WDR35 المسببة لخلل التنسج القحفي الظاهر النوع 2، وتعد شجرة العائلة ضرورية لتقييم خطورة التكرار الوراثي.
2. How is the sample collected and what are the accepted sample types?
We accept whole blood, extracted DNA, or a one-drop dried blood spot on an FTA card; a certified phlebotomist will perform painless home collection using ISO cold-chain transport to preserve DNA integrity. نقبل عينات الدم الكامل أو الحمض النووي المستخلص أو بقعة دم جافة على بطاقة FTA، حيث يقوم أخصائي معتمد بسحب العينة منزلياً مع نقلها وفق سلسلة تبريد الآيزو.
3. Is a genetic counseling session mandatory before testing?
Pre- genetic counseling is mandatory to document the clinical history, construct a pedigree, and ensure informed consent; our service includes this session at no extra cost, conducted virtually via telehealth in English or Arabic. جلسة الاستشارة الوراثية قبل الفحص إلزامية لتوثيق التاريخ السريري ورسم شجرة العائلة وضمان الموافقة المستنيرة، وتُقدم مجاناً عبر الإنترنت بالعربية أو الإنجليزية.
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians