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Test Price

2,000 AED

✅ Home Collection Available

Spinocerebellar Ataxia (SCA) Genetic Panel (Types 1, 2, 3, 6, 7, 10 & 12) in UAE | 2,000 AED | DNA Labs UAE

Executive Summary & Core Metrics

  • Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing.
  • Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
  • Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation by a DHA-licensed Consultant Medical Geneticist.
  • Direct Billing: Insurance verification and direct billing support available via WhatsApp at +971 54 548 8731.
  • DHA Licensed Facility: Performed under DHA Facility License Number 1143 at DNA Labs UAE, Dubai Healthcare City.

Test Overview & Methodology

The Spinocerebellar Ataxia (SCA) Genetic Panel is a targeted molecular diagnostic test that analyzes seven of the most common genetic subtypes (Types 1, 2, 3, 6, 7, 10, and 12). This test confirms the clinical diagnosis of hereditary ataxia, provides essential prognostic information, and facilitates informed family planning and genetic counseling. The test employs highly sensitive techniques to detect abnormal trinucleotide repeat expansions within the specific SCA-associated genes.

Performance & Logistical Comparison

Feature DNA Labs UAE SCA Panel Standard Hospital Alternative
Precision Methodology Triplet Repeat Primed PCR (TP‑PCR) & Fragment Analysis by Capillary Electrophoresis Conventional End‑Point PCR only
Turnaround Time 5-7 Business Days 10-14 Business Days
DHA‑Licensed Counselling Included (Telephonic Consultation) Often referral‑based only
Home Collection Logistics VIP Mobile Phlebotomy & ISO‑Certified Cold‑Chain, 8 AM‑11 PM Limited hours, no guaranteed cold chain

Physician Insight & Safety Protocols

“As a Consultant in Medical Genetics, I emphasize that comprehensive genetic panel testing for SCA provides a definitive molecular diagnosis crucial for prognosis and family planning. However, the interpretation of these findings must always be contextualized within the patient's complete neurological history and family pedigree. I strongly advise all patients to undergo a formal post-test genetic counseling session to fully understand the implications for themselves and their relatives before making any life-altering decisions.”

— Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403

Clinical Advisory

Medication Advisory: Do not discontinue, alter, or initiate any prescribed neurological medication without prior consultation with your treating physician. Changes in therapy should only be made based on a comprehensive clinical evaluation.

Patient Safety & Exclusion Criteria

  • Exclusion Criteria: This test is not recommended for asymptomatic minors without formal genetic counseling and informed parental consent. Pregnancy must be declared; testing is only conducted when medically indicated and ordered by the managing physician. Specimens exhibiting significant hemolysis or insufficient volume will be rejected.
  • Emergency Red Flags – Seek Immediate Medical Attention: Sudden onset of severe gait imbalance, new difficulty swallowing (dysphagia), double vision (diplopia), or altered consciousness.

Patient FAQ & Clinical Guidance

1. What is the Spinocerebellar Ataxia Genetic Panel and why is it performed?

This panel simultaneously analyzes seven specific genes associated with dominant hereditary ataxias. It is performed to confirm a clinical diagnosis of SCA, determine the exact genetic subtype for prognosis, evaluate carrier status, and inform family planning decisions.

2. How should I prepare for the sample collection?

No fasting or special preparation is required. A routine peripheral whole blood sample (approximately 3-5 ml) will be collected using standard aseptic venipuncture techniques. This can be performed at your home by a licensed phlebotomist or at our facility in Dubai Healthcare City.

3. What support will I receive after my results are ready?

You will be provided with a detailed molecular report. A DHA-licensed Consultant Medical Geneticist will schedule a telephonic consultation to interpret the report, explain the clinical significance of any identified variants, and recommend appropriate management or further genetic counseling for you and your family.

UAE Regulatory & Data Privacy Adherence

Secure and Compliant Diagnostics

DNA Labs UAE strictly adheres to the Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) for the secure processing, storage, and transmission of your genetic information. Our laboratory operations and clinical workflows fully comply with Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, ensuring the highest standards of digital health security and patient data confidentiality. Clinical safety and patient consent protocols align with Federal Decree-Law No. 4 of 2016 on Medical Liability.

Clinical & Logistical Metadata

Test Name Spinocerebellar Ataxia (SCA) Genetic Panel (Types 1, 2, 3, 6, 7, 10 & 12)
Price (AED) 2,000 AED
Turnaround Time 5-7 Business Days
Sample Type / Matrix Peripheral Whole Blood
Methodology Used Triplet Repeat Primed PCR (TP-PCR) & Fragment Analysis by Capillary Electrophoresis
ICD-10-CM Code G11.0, Z13.71
LOINC Code 86210-1
DHA Facility License & Address License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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