Test Price
1,400 AED✅ Home Collection Available
FISH Prenatal Screening Panel (Chromosomes 13, 18, 21, X & Y) in UAE | 1400 AED | 2026 DHA Guidelines
تحليل لوحة فحص ما قبل الولادة بتقنية FISH للكروموسومات 13 و18 و21 وX وY في الإمارات | 1400 درهم | معتمد من هيئة الصحة بدبي
Executive Summary – الملخص التنفيذي
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: Paid Hospital-Grade Home Collection via ISO Certified Cold-Chain Home Collection and VIP Mobile Phlebotomy (8 AM – 11 PM daily).
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation from DHA-licensed obstetric counsellors.
- Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
- الالتزام التنظيمي: الامتثال الكامل للمرسوم بقانون اتحادي رقم 41 لسنة 2024 (المادة 87)، وقانون الخدمات العلاجية الرقمية للقُصَّر 2026، وقانون حماية البيانات الشخصية في الإمارات.
Overview
The FISH Prenatal Screening Panel rapidly rules out the most common chromosomal aneuploidies—trisomy 13, 18, 21 (Down syndrome), and sex chromosome abnormalities (X & Y)—directly on uncultured amniotic fluid cells. توفر لوحة FISH قبل الولادة كشفًا سريعًا لاختلالات الكروموسومات 13 و18 و21 والصبغيات الجنسية (X/Y) من عينة السائل الأمنيوسي دون زراعة خلايا، مما يمنح الآباء إجابات مبكرة ودقيقة.
| Feature | Our FISH Panel (UAE) | Conventional Karyotype |
|---|---|---|
| Result Turnaround | 4 Days (Report by 4 pm) | 10–14 Days |
| Methodology | FISH (Interphase Nuclei Analysis) | Culture-dependent G-Banding |
| Diagnostic Scope | 5 critical aneuploidies (13,18,21,X,Y) | All chromosome number >5 Mb structural |
| Clinical Applicability | Rapid risk stratification in high-risk pregnancy | Confirmatory comprehensive analysis |
Physician Insight & Safety Protocol
"As a DHA-licensed obstetrician, I emphasize that a positive FISH result must be integrated with ultrasound findings and clinical history; a negative FISH never fully excludes mosaic aneuploidy or microdeletions, so confirmatory karyotype or microarray is often indicated." – Dr. PRABHAKAR REDDY (DHA: 61713011)
"This panel provides rapid clarity for anxious parents, but it is not a stand-alone diagnosis. We always correlate with detailed second-trimester morphology scan and maternal serum screening results." – Dr. PRABHAKAR REDDY
"For high-risk pregnancies identified by NIPT or advanced maternal age, FISH on amniocytes offers a diagnostic answer within days, reducing the period of uncertainty." – Dr. PRABHAKAR REDDY
⚠ Medication & Clinical Safety Warning
Do not discontinue any prescribed medication or prenatal supplement without consulting your managing obstetrician or maternal-fetal medicine specialist.
This test requires informed consent and specific clinical forms. Any invasive diagnostic procedure carries a small risk of miscarriage; it must be performed by a qualified operator under ultrasound guidance. If you experience cramping, vaginal bleeding, or fluid leakage after the procedure, seek emergency obstetric evaluation immediately.
Exclusion Criteria & Emergency Red Flags
- Active vaginal bleeding or confirmed ruptured membranes before amniocentesis.
- Multiple gestation with chorionicity not clearly established.
- Maternal coagulation disorder or anticoagulant therapy not cleared by haematologist.
- Gestational age <15 weeks (amniocentesis not recommended).
- Red Flags after sample collection: fever >38°C, severe abdominal pain, or decreased fetal movements; proceed to nearest ER.
Patient FAQ & Clinical Guidance
Q: What is the FISH prenatal screening panel and what does it detect?
Snippet Answer: The FISH prenatal panel directly identifies abnormal copy numbers of chromosomes 13, 18, 21, X, and Y in uncultured amniotic fluid cells, delivering results within 4 days for the most common aneuploidies associated with severe developmental disorders.
تكتشف لوحة FISH قبل الولادة بدقة وسرعة اختلالات عدد الكروموسومات 13 و18 و21 والصبغيات الجنسية (X/Y) مباشرة من خلايا السائل الأمنيوسي، مما يسمح بالتدخل المبكر واتخاذ القرارات المستنيرة.
Q: How is the test performed and is it safe for the mother and baby?
Snippet Answer: A trained specialist extracts 10 mL of amniotic fluid under continuous ultrasound guidance after 15 weeks of gestation, a procedure with an overall procedural risk of less than 1 in 500 when performed by an experienced operator in a DHA-licensed facility.
يتم سحب 10 مل من السائل الأمنيوسي تحت توجيه الموجات فوق الصوتية بعد الأسبوع 15 من الحمل، وتكون نسبة الخطر أقل من 0.2% عند إجرائها على يد أخصائي خبير.
Q: When should this test be done and what do the results mean?
Snippet Answer: The is indicated for pregnancies with high-risk non-invasive prenatal testing (NIPT) results, advanced maternal age, or ultrasound markers suggestive of aneuploidy, and a positive signal mandates genetic counselling before any pregnancy management decision.
ينصح بالاختبار إذا أظهرت فحوصات NIPT خطراً مرتفعاً أو عند تقدم سن الأم أو وجود علامات في السونار، ويجب تفسير النتائج من قبل طبيب مختص لاتخاذ القرار المناسب.
For comprehensive prenatal genetic counselling or to schedule your DHA-compliant amniocentesis, contact our 24/7 WhatsApp support at +971 54 548 8731. Home collection services operate 8 AM – 11 PM across all Emirates.
Facility License: 9834453 | ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139) | This panel adheres to Federal Decree-Law No. 41 of 2024 (Art. 87), UAE CDS Law 2026 (Minors), and UAE PDPL. All genetic data is processed in-country with full privacy compliance.
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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.
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