Test Price
2,800 AED✅ Home Collection Available
SARDH Gene Sarcosinemia Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين SARDH لساركوزينيميا NGS في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary: Guaranteed Diagnostic Excellence
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited NGS Processing.
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection for DNA samples. VIP Mobile Phlebotomy available 8 AM – 11 PM.
- Clinical Guidance: Complimentary Telephonic Post-Test Clinical Guidance in result interpretation by DHA-licensed specialists.
- Insurance: Quick Direct Billing Verification via WhatsApp +971 54 548 8731.
ملخص تنفيذي: يضمن هذا الاختبار الجيني التشخيصي للساركوزينيميا دقة عالية بنسبة 99.9% من خلال تحليل تسلسل الجيل التالي (NGS) المعتمد وفق معايير ISO، مع خدمة سحب عينات منزلية محترفة وإرشاد طبي هاتفي بعد النتائج. التحقق من التأمين عبر واتساب.
Comprehensive SARDH Gene Sarcosinemia Genetic Test Overview
This advanced Next-Generation Sequencing (NGS) test deciphers your entire SARDH gene for pathogenic variants linked to sarcosinemia, a rare inborn error of amino acid metabolism. يقوم هذا التحليل الجيني المتطور بتسلسل كامل جين SARDH للكشف عن الطفرات المسببة للساركوزينيميا، وهو اضطراب استقلابي وراثي نادر.
Designed for patients with unexplained neurological symptoms, metabolic acidosis, or family history, it offers definitive molecular diagnosis unmatched by traditional metabolic screens. Recommended by General Physicians, Clinical Geneticists, and Metabolic Disease Specialists.
| Feature | Our Test: SARDH NGS DNA | Closest Alternative: Tandem MS/MS Metabolic Screen |
|---|---|---|
| Precision | 99.9% Diagnostic Sensitivity for SARDH mutations; identifies all variant types (missense, nonsense, splice-site, deletions). | Only quantifies sarcosine and sarcosine:creatinine ratio; cannot distinguish genetic subtypes. |
| Methodology | Next-Generation Sequencing (Illumina® Novaseq™) with Sanger confirmation & bioinformatic analysis aligned to 2026 ClinVar/ACMG guidelines. | Tandem Mass Spectrometry (MS/MS) – biochemical screening. |
| Turnaround Time | 3–4 Weeks (comprehensive report with genetic counseling referral). | 48–72 hours (rapid but non-confirmatory). |
Physician Insight & Safety Protocol
“As a DHA-licensed clinician, I emphasize that this genetic test is a powerful tool for confirming sarcosinemia, yet it must always be correlated with clinical symptoms and biochemical findings. No test replaces the art of medicine—listen to your patient’s story. Do not stop prescribed therapies without consultation.”
— Dr. PRABHAKAR REDDY, DHA License 61713011
⚠️ Critical Safety Information
Exclusion Criteria
- Inability to provide informed consent (or minor without legal guardian consent as per UAE Child Data Safeguarding Law 2026).
- Unwillingness to participate in mandatory pre-test genetic counseling session.
- Acute intercurrent illness with fever >38.5°C – reschedule to avoid stress on sample quality.
🚑 Emergency Red Flags
- Sudden severe vomiting, lethargy, or altered consciousness – potential metabolic crisis.
- Progressive developmental regression or new-onset seizures.
- Signs of acute acidosis (rapid breathing, confusion).
- Seek immediate hospital care; do not wait for this test result.
Medication Warning: Do not discontinue any prescribed medication (e.g., sodium benzoate, anti-epileptics) without consulting your treating physician. Genetic results may impact management but require medical supervision.
Patient Frequently Asked Questions & Clinical Guidance
What is the SARDH gene sarcosinemia Genetic Test, and why is it done?
The SARDH Genetic Test scans your full SARDH gene for mutations linked to sarcosinemia, an amino acid metabolism defect.
يقوم اختبار جين SARDH بتسلسل الحمض النووي الكامل للكشف عن الطفرات المسببة للساركوزينيميا، وهو اضطراب استقلابي وراثي نادر.
This test is indicated when a patient presents with developmental delay, speech impairment, intellectual disability, or unexplained elevated sarcosine on newborn screening. It confirms a molecular diagnosis and helps guide dietary management and genetic family planning.
How is the sample collected, and are there special preparations?
A simple blood draw (whole blood) or DNA FTA card is collected at home by our cold-chain phlebotomist.
يتم جمع عينة دم بسيطة (دم كامل) أو بقعة دم على بطاقة FTA منزليًا بواسطة فني سحب محترف مع سلسلة تبريد مضمونة.
No fasting is required for genomic DNA. However, a mandatory pre- genetic counseling session will record your clinical history and draw a pedigree chart to improve interpretation. All personal data is protected under UAE PDPL and Federal Decree-Law No. 41 of 2024.
What do the results mean, and how will I receive them?
A DHA-licensed genetic counselor will explain the presence or absence of pathogenic SARDH variants and inherited pattern.
سيشرح مستشار وراثي مرخص من هيئة الصحة بدبي وجود الطفرات المرضية في جين SARDH ونمط الوراثة.
You will receive a digitally signed report within 3–4 weeks via our secure portal. Results include detailed variant classification according to ACMG guidelines (Pathogenic, Likely Pathogenic, VUS). A 30-minute telephonic interpretation session is included to discuss next steps, including referral to a metabolic specialist if positive.
دعم ثنائي اللغة متاح
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
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All reports reviewed by DHA-Certified physicians