Test Price
2,800 AED✅ Home Collection Available
HOXD13 Gene Syndactyly Type 5 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
DHA-Approvedتحليل جين HOXD13 لمتلازمة الأصابع الملتصقة من النوع الخامس في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
الملخص التنفيذي: يضمن هذا الاختبار الجيني المتطور تسلسل الجيل التالي (NGS) لتحديد الطفرات في جين HOXD13 المرتبطة بمتلازمة الأصابع الملتصقة من النوع الخامس (Syndactyly Type 5)، بدقة تشخيصية تصل إلى 99.9% من خلال مختبر معتمد وفقًا لمعيار الآيزو 9001:2015. تشمل الخدمة سحب الدم المنزلي وفق سلسلة تبريد معتمدة، واستشارة طبية هاتفية بعد صدور النتيجة.
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview
The HOXD13 Gene Syndactyly Type 5 Genetic Test utilizes next-generation sequencing to detect pathogenic variants in the HOXD13 gene, confirming a clinical diagnosis of syndactyly type 5 (SD5) and guiding family planning. This test is essential for pediatricians, clinical geneticists, and genetic counselors managing congenital limb malformations. يعد هذا الاختبار أساسيًا لتأكيد التشخيص وتوجيه الإرشاد الوراثي.
| Feature | Our Test | Closest Alternative |
|---|---|---|
| Precision | NGS with 100% coverage of HOXD13 coding regions | Sanger sequencing (single exon focus) |
| Methodology | Next-Generation Sequencing (Illumina platform, ISO validated) | Sanger sequencing |
| Turnaround Time | 3–4 weeks | 4–6 weeks |
Physician Insight & Safety Protocol
“As a seasoned clinical geneticist, I emphasize that a positive HOXD13 variant must be interpreted in the context of clinical and family history. This test offers clarity for families, but it should never replace thorough physical examination and genetic counseling.” — Dr. PRABHAKAR REDDY, DHA License 61713011.
⚠️ Do not discontinue prescribed medication without consulting your doctor. This genetic test does not replace clinical management.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Inability to provide informed consent; severe coagulopathy; active skin infection at venipuncture site.
- Exclusion: Patient undergoing high-dose anticoagulant therapy (relative; discuss with physician).
- ER Red Flag: If the affected limb develops sudden swelling, discoloration, or severe pain, seek immediate surgical evaluation—this test is not for acute crisis.
Patient FAQ & Clinical Guidance
1. English: What is the HOXD13 gene test used for? ما هو استخدام تحليل جين HOXD13؟
Direct Answer: This test identifies mutations in the HOXD13 gene to confirm a diagnosis of syndactyly type 5, a hereditary hand malformation.
It provides definitive molecular confirmation, enabling accurate genetic counseling and recurrence risk assessment for family members. The is recommended when physical exam suggests SD5 and there is a positive family history.
2. English: How is the sample collected, and is it painful? كيف يتم جمع العينة وهل هي مؤلمة؟
Direct Answer: A simple blood draw or a painless finger-stick onto an FTA card is performed by a trained phlebotomist.
Our home collection team follows strict cold-chain protocols; the process takes less than 10 minutes and is suitable for children with minimal discomfort. No special preparation is needed beyond a genetic counselling session to document the family pedigree.
3. English: When will I receive my results, and what support is provided? متى سأحصل على نتائجي وما الدعم المقدم؟
Direct Answer: Results are delivered within 3 to 4 weeks, accompanied by a telephonic consultation with a clinical geneticist.
We provide a comprehensive report explaining the genetic finding and its implications, plus direct access to a genetic counselor to discuss next steps, including potential surgical interventions or family planning.
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians