Test Price
2,800 AED✅ Home Collection Available
SGCD Gene Limb‑Girdle Muscular Dystrophy Type 2F Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين SGCD للضمور العضلي الحزامي الطرفي (النوع 2F الصبغي الجسدي المتنحي) بتقنية التسلسل الجيني المتطور (NGS) في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
🔬 Premium LGMD2F Genetic Profiling – Accuracy Guaranteed
- 99.9% Diagnostic Sensitivity – NGS sequencing of the entire SGCD coding region, validated under ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).
- VIP Home Phlebotomy – Hospital-grade sample collection via cold‑chain transport, 8 AM–11 PM daily.
- Post‑Test Clinical Guidance – Complimentary tele‑consult to explain your results and next steps.
- Insurance & Billing – Direct verification via WhatsApp at +971 54 548 8731.
الملخص التنفيذي
يقدم هذا الفحص تحليلاً جينياً متكاملاً للكشف عن الطفرات المرضية في جين SGCD المسبب للضمور العضلي الحزامي الطرفي النوع 2F، بتقنية NGS وبدقة تشخيصية تبلغ 99.9%، معتمداً من هيئة الصحة بدبي ومطابقاً للمرسوم بقانون اتحادي رقم 41 لسنة 2024. تشمل الخدمة السحب المنزلي والتوصيل المبرد بمواصفة ISO 9001:2015، وجلسة استشارة وراثية هاتفية بعد الفحص.
Comprehensive SGCD Gene Analysis for Autosomal Recessive LGMD2F
Overview: Limb‑Girdle Muscular Dystrophy Type 2F (LGMD2F) is an autosomal recessive neuromuscular disorder caused by biallelic loss‑of‑function variants in the SGCD (δ‑sarcoglycan) gene. This NGS‑based assay interrogates all coding exons and flanking splice sites to enable definitive diagnosis, carrier detection, and family risk assessment – essential for proactive neuromuscular management.
| Feature | Our Test (SGCD NGS) | Closest Alternative (Sanger Sequencing) |
|---|---|---|
| Precision / Sensitivity | 99.9% clinical sensitivity; full gene coverage with uniform depth >100× | ~98% for targeted mutations; may miss large deletions/insertions |
| Methodology | Next-Generation Sequencing (Illumina® platform) + bioinformatic analysis per ACMG 2026 | Capillary electrophoresis, single‑exon approach |
| Turnaround Time | 3 – 4 weeks (standard) | 4 – 6 weeks |
| Sample Type | Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA® card) | Blood or DNA only |
Physician Insight & Safety Protocol
Dr. PRABHAKAR REDDY (DHA License: 61713011) explains:
“LGMD2F often presents with progressive pelvic‑shoulder weakness, calf hypertrophy, and elevated CK levels. The SGCD NGS test provides molecular confirmation that differentiates this subtype from other LGMDs and guides cardiac and respiratory surveillance. Please remember that a genetic result must always be correlated with your clinical picture and family history – never self‑interpret.”
⚠️ Medication Safety & Clinical Exclusion
- Do not discontinue any prescribed medication (e.g., corticosteroids, cardiac drugs) without your neurologist’s approval.
- Exclusion criteria: Active infection, recent vaccination, or current use of anticoagulants (relative) – discuss with our phlebotomist before home collection.
- Emergency red flags: If you experience sudden difficulty breathing, chest pain, or acute loss of ambulation, seek emergency care immediately. This test is not a substitute for acute medical evaluation.
Patient FAQ & Clinical Guidance
Q: What conditions does the SGCD gene test detect?
Snippet Answer: The SGCD gene NGS definitively identifies biallelic mutations causing autosomal recessive limb‑girdle muscular dystrophy type 2F, enabling accurate diagnosis and family planning.
س: هل يمكن إجراء الفحص للأطفال القُصّر؟
إجابة موجزة: نعم، يُسمح بإجراء تحليل جين SGCD للأطفال والمراهقين عند وجود أعراض سريرية أو تاريخ عائلي، وفقاً لقانون البيانات الصحية للقاصرين في دولة الإمارات لعام 2026، وبعد الحصول على موافقة الوالدين وجلسة استشارة وراثية.
Q: How long does it take to receive results, and how will I get them?
Snippet Answer: Standard reporting time is 3 to 4 weeks; your DHA‑compliant digital report is delivered via encrypted email, followed by a physician‑led tele‑consultation to explain findings and next‑steps.
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