Test Price
2,800 AED✅ Home Collection Available
LARS2 Gene Hydrops, Lactic Acidosis, and Sideroblastic Anemia (HLASA) Genetic Test in UAE | 2800 AED | 2026 DHA Guidelines
تحليل جين LARS2 للاستسقاء والحماض اللبني وفقر الدم الأرومي الحديدي في الإمارات | 2800 درهم | معتمد من هيئة الصحة بدبي
99.9% Diagnostic Sensitivity via ISO Certified Processing
Paid Hospital-Grade Home Collection via ISO Cold-Chain Home Collection & VIP Mobile Phlebotomy
Telephonic Post-Test Clinical Interpretation Support
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Overview
The LARS2 NGS test precisely identifies pathogenic variants in the LARS2 gene, confirming Hydrops, Lactic Acidosis, and Sideroblastic Anemia (HLASA) syndrome. يحدد التحليل الجيني الطفرات المسببة لمتلازمة الاستسقاء والحماض اللبني وفقر الدم الأرومي الحديدي، وهو اضطراب ميتوكوندري نادر.
| Features | Our HLASA NGS Test | Standard Sanger Panel |
|---|---|---|
| Genetic Coverage | Full LARS2 gene sequencing + CNV detection | Limited to selected exons, missing copy number changes |
| Methodology | Next Generation Sequencing (NGS) – high sensitivity | Sanger sequencing – lower throughput |
| Turnaround Time | 3–4 Weeks (comprehensive report) | 4–6 Weeks or longer for multiple exons |
Physician Insight & Safety Protocol
"This test provides genetic clarity for a rare but serious condition that can affect pregnancy and hematologic health. It is crucial to interpret results alongside clinical findings and a detailed family history. I recommend genetic counselling before and after testing to ensure informed decision-making."
— Dr. PRABHAKAR REDDY, Consultant Hematologist, DHA License 61713011
Medication Warning
Do not discontinue prescribed medication without consulting your doctor. Genetic test results must be reviewed by a licensed clinician before any treatment adjustment.
Exclusion Criteria & Emergency Red Flags
- Age under 18 years without parental/guardian consent and presence.
- Acute febrile illness or clinically unstable condition requiring hospital monitoring.
- Inability to provide a viable blood/DNA sample (severe thrombocytopenia/coagulopathy).
- Refusal of pre-test genetic counselling as mandated by CDS Law 2026 for minors.
- Severe anemia symptoms: chest pain, shortness of breath, dizziness, or syncope.
- Signs of hydrops: rapid weight gain, respiratory distress, pallor, or edema.
- Persistent lactic acidosis signs: deep, rapid breathing, confusion, extreme fatigue.
- Any sudden deterioration—call 998 immediately.
Patient FAQ & Clinical Guidance
What is the LARS2 gene test used for?
Identifying LARS2 gene mutations enables precise diagnosis of HLASA syndrome, guiding clinical management and family planning.
تحديد طفرات جين LARS2 يُمكّن من تشخيص دقيق لمتلازمة الاستسقاء والحماض اللبني وفقر الدم الأرومي الحديدي، وتوجيه الرعاية السريرية والتخطيط الأسري.
How is the test performed?
NGS sequencing of blood, extracted DNA, or FTA card sample detects LARS2 gene mutations reliably.
يتم تحليل عينة الدم أو الحمض النووي المستخلص أو بقعة الدم على بطاقة FTA بتقنية التسلسل من الجيل التالي لكشف طفرات جين LARS2 بدقة.
When will I receive the results?
Receive your LARS2 gene analysis results in 3–4 weeks, with dedicated post-test clinical guidance call.
تستلم نتائج تحليل جين LARS2 خلال 3 إلى 4 أسابيع مع جلسة إرشاد هاتفية بعد الاختبار لشرح التقرير.
Regulatory Compliance: This service complies with Federal Decree-Law No. 41 of 2024 (Art. 87), CDS Law 2026 (Genetic Testing in Minors), and UAE PDPL. Accredited under ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139). DHA Facility License #9834453.
Important: Pre- genetic counselling is mandatory; a pedigree chart of family members affected by LARS2‑related HLASA is required. Do not alter medications without your doctor’s approval.
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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
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All reports reviewed by DHA-Certified physicians