Test Price
2,800 AED✅ Home Collection Available
FLNA Gene FG Syndrome Type 2 Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين FLNA لمتلازمة FG من النوع 2 في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
Executive Summary
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Certified Laboratory & NGS Technology
- 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 for result interpretation included
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731
ملخص تنفيذي: يضمن فحص تسلسل الجيل التالي (NGS) لجين FLNA تشخيصاً دقيقاً لمتلازمة FG من النوع 2، المرتبطة بطفرات جينية تسبب تشوهات دماغية وتأخراً نمائياً. يُجرى الفحص وفق أعلى معايير هيئة الصحة بدبي لعام 2026، مع خدمة سحب دم منزلي بسلسلة تبريد معتمدة ISO، واستشارة وراثية هاتفية بعد النتيجة.
Comprehensive Genetic Insight for Neurological Disorders
The FLNA NGS test screens the entire coding region of the filamin A gene for pathogenic variants linked to FG syndrome type 2, a condition characterised by periventricular nodular heterotopia, epilepsy, and connective tissue anomalies. يوفر هذا التحليل تشخيصاً جزيئياً دقيقاً يدعم استشارة الوراثة الطبية وتخطيط الرعاية المستقبلية.
| Feature | Our Test – FLNA NGS | Closest Alternative – Sanger Sequencing |
|---|---|---|
| Precision | Full gene sequencing + copy number variants | Targeted mutation hotspots only |
| Method | NGS (Next‑Generation Sequencing) | Sanger sequencing |
| Turnaround | 3 – 4 Weeks | 6 – 8 Weeks |
| Clinical Yield | Detects 99% of pathogenic FLNA variants | Limited to known familial mutations |
Clinician’s Perspective & Safety Protocol
“As a neurologist who has accompanied many families through the diagnostic odyssey, I want you to know that this test is a powerful step toward clarity. A positive result may finally explain your child’s symptoms, yet every genetic finding must be woven together with their clinical picture – imaging, EEG, and the unique story of your family. We are here to translate that complex result into a compassionate care plan.”
— Dr. PRABHAKAR REDDY, DHA Lic. 61713011
⚠️ Medication Warning: Do not discontinue prescribed medication without consulting your doctor.
Exclusion Criteria & Emergency Information
- Severe coagulopathy or active bleeding disorder
- Acute febrile illness or systemic infection at time of collection
- Known lack of venous access requiring specialised line placement
ER Red Flags: If you experience heavy bleeding, expanding haematoma, or signs of infection after blood draw, seek immediate medical attention. Worsening of neurological symptoms – prolonged seizures, altered consciousness – should trigger an emergency room visit.
Patient FAQ & Clinical Guidance
1. What is FLNA gene FG syndrome type 2 and how does this test help?
FLNA gene FG syndrome type 2 is a rare X-linked disorder causing brain malformations, developmental delay, and connective tissue symptoms. This NGS identifies disease‑causing variants in the FLNA gene, confirming a clinical suspicion and enabling personalised surveillance. يُحدد الاختبار الطفرات المسببة للمرض في جين FLNA المرتبط بتشوهات العقد الرمادية حول البطينات.
2. How is the sample collected and what preparation is needed?
We collect a small blood sample (or one drop on FTA card) through a painless, at‑home phlebotomy service with cold‑chain transport. No fasting is required; however, a prior genetic counselling session to document family pedigree is mandatory. تُؤخذ العينة بسحب دم بسيط في المنزل؛ مع ضرورة جلسة استشارة وراثية مسبقة لرسم شجرة العائلة.
3. How long do results take and who interprets them?
Results are ready in 3 to 4 weeks and are interpreted by a board‑certified neurologist or clinical geneticist during a tele‑consultation. The report includes a clear clinical correlation note and actionable recommendations. تظهر النتائج خلال 3 إلى 4 أسابيع ويُفسرها طبيب أعصاب أو اختصاصي وراثة معتمد عبر استشارة هاتفية.
Facility License: 9834453 | ISO 9001:2015 Certified (Cert: INT/EGQ/2509DA/3139)
Compliance: Federal Decree‑Law No. 41 of 2024 (Art. 87), UAE CDS Law 2026, UAE PDPL
Home Collection: 8 AM – 11 PM | WhatsApp Support: +971545488731
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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
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All reports reviewed by DHA-Certified physicians