Skip to main content

Genetics

Spinocerebellar Ataxia Tests in Dubai & UAE

Investigations in this area, with the specimen type, turnaround time and listed price for each option — so you and your clinician can compare before you book.

3 min read
View investigations
  • Quality-controlled laboratory
  • Home collection across the UAE
  • Confidential handling of results

Compare options

Spinocerebellar Ataxia investigations

All 14 investigations in this category are listed below.

Spinocerebellar Ataxia tests offered by DNA Labs UAE — compare specimen type, turnaround time and listed price. Preparation and clinical interpretation are confirmed with your clinician before collection.
Test What it measures Specimen Turnaround Price Book
ANO10 Gene Spinocerebellar Ataxia Type 10, Autosomal Recessive Genetic Test TEST-5848 LOINC 21657-1 This test evaluates the ANO10 gene for pathogenic variants associated with autosomal recessive spinocerebellar ataxia type 10 (SCAR10). It identifies... Whole Blood, Extracted DNA, or One Drop of Blood on an FTA Card 3 to 4 Weeks 2,800.00 AED Details
ATP2B3 Gene Spinocerebellar Ataxia Type 1 (X‑Linked) Genetic Test TEST-5844 LOINC 21643-9 This genetic test evaluates the ATP2B3 gene for mutations associated with X-linked spinocerebellar ataxia type 1. Peripheral whole blood (EDTA tube), extracted DNA, or FTA card 3–4 weeks 2,800.00 AED Details
ATXN1 Gene Spinocerebellar Ataxia Type 1 (SCA1) Autosomal Dominant Genetic Test TEST-5737 LOINC 94880-2 This test identifies pathogenic CAG trinucleotide repeat expansions in the ATXN1 gene, confirming a diagnosis of Autosomal Dominant Spinocerebellar At... Peripheral Whole Blood (5 mL) 3–4 Weeks 2,800.00 AED Details
FGF14 Gene Spinocerebellar Ataxia Type 27 (Autosomal Dominant) Genetic Test TEST-5778 LOINC 55233-1 This genetic test evaluates the FGF14 gene for pathogenic variants associated with autosomal dominant spinocerebellar ataxia type 27 (SCA27). Peripheral Blood 3-4 Weeks 2,800.00 AED Details
GRM1 Gene Spinocerebellar Ataxia Type 13, Autosomal Recessive Genetic Test TEST-5754 LOINC 21615-1 This test identifies pathogenic variants in the GRM1 gene associated with autosomal recessive Spinocerebellar Ataxia Type 13. Whole Blood, Extracted DNA, or Dried Blood Spot (FTA Card) 3 – 4 Weeks 2,800.00 AED Details
IFRD1 Gene Spinocerebellar Ataxia Type 18 (Autosomal Dominant) Genetic Test TEST-5867 LOINC 81325-1 This test identifies pathogenic variants in the IFRD1 gene associated with autosomal dominant spinocerebellar ataxia type 18. Peripheral whole blood (3 mL EDTA) 3–4 weeks 2,800.00 AED Details
KCNC3 Gene Spinocerebellar Ataxia Type 13 (Autosomal Dominant) Genetic Test TEST-5855 LOINC 55233-1 This test analyzes the KCNC3 gene to identify pathogenic variants associated with Spinocerebellar Ataxia Type 13 (SCA13). It confirms the genetic basi... Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot 3 – 4 weeks 2,800.00 AED Details
KCND3 Gene Spinocerebellar Ataxia Type 22 (Autosomal Dominant) Genetic Test TEST-5876 LOINC 101061-1 This test identifies mutations in the KCND3 gene associated with autosomal dominant Spinocerebellar Ataxia Type 22 (SCA22). Whole Blood (EDTA) • Extracted DNA • Dried Blood Spot (FTA Card) 3–4 Weeks 2,800.00 AED Details
NOP56 Gene Spinocerebellar Ataxia Type 36 (SCA36) Autosomal Dominant Genetic Test TEST-5793 LOINC 81317-5 This test detects pathogenic GGCCTG hexanucleotide repeat expansions in the NOP56 gene, confirming a diagnosis of Spinocerebellar Ataxia Type 36 (SCA3... Peripheral whole blood (EDTA tube) 3–4 Weeks from sample receipt 2,800.00 AED Details
PLEKHG4 Genetic SCA4 Test TEST-5891 LOINC 21684-4 This test identifies pathogenic variants in the PLEKHG4 gene associated with Spinocerebellar Ataxia Type 4 (SCA4). It provides definitive molecular co... Whole Blood (Peripheral), Extracted DNA, or One Drop Blood on FTA Card 3–4 Weeks 2,800.00 AED Details
PRKCG Gene Spinocerebellar Ataxia Type 14 (Autosomal Dominant) Test TEST-5859 LOINC 81247-7 This genetic test identifies pathogenic variants in the PRKCG gene associated with autosomal dominant Spinocerebellar Ataxia Type 14 (SCA14). Whole Blood, Extracted DNA, or FTA Card (One Drop Blood) 3–4 weeks from sample receipt 2,800.00 AED Details
SCA‑14 (PRKCG Gene Mutation) Test TEST-3065 LOINC 98590-0 This test identifies pathogenic variants in the PRKCG gene associated with autosomal dominant spinocerebellar ataxia type 14. Whole Blood (EDTA) 10-12 Business Days 1,500.00 AED Details
SCA11 (Spinocerebellar Ataxia Type 11) Test TEST-3061 LOINC 93969-6 This test identifies pathogenic variants in the TTBK2 gene associated with Spinocerebellar Ataxia Type 11 (SCA11). It provides definitive genotypic ev... EDTA Whole Blood (Peripheral) 10–12 business days from specimen receipt 1,200.00 AED Details
SPTBN2 Gene Sequencing (Spinocerebellar Ataxia Type 5, Autosomal Dominant) Test TEST-5798 LOINC 94547-4 This test identifies pathogenic variants in the SPTBN2 gene to diagnose autosomal dominant spinocerebellar ataxia type 5 (SCA5). Peripheral Whole Blood (3–5 mL in EDTA tube) 3–4 weeks 2,800.00 AED Details

Clinical overview

About Spinocerebellar Ataxia

Confronting progressive loss of coordination, balance issues, or a family history of movement disorders can be deeply unsettling, but precise genetic factors provide a clear path forward. Within our advanced neurogenetics department, Spinocerebellar Ataxia (SCA) testing meticulously evaluates your DNA for the specific trinucleotide repeats or mutations causing this progressive neurological condition. Utilizing cutting-edge diagnostic technology, this highly focused molecular screening clarifies the hereditary nature of your symptoms, safely guiding personalized neurological care, physical therapy, and proactive family planning. Recognized for neurogenetic excellence among premier diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, exceptional diagnostic accuracy, and rapid reporting. Take an informed step in your neurological health—schedule your spinocerebellar ataxia testing in UAE, book a secure home sample collection, or consult our expert neurology genetics specialists.

Before your appointment

Preparation & sample collection

Follow the instructions you are given

Fasting, timing and medicine restrictions differ between investigations. The instructions for your specific request are confirmed when you book.

Bring your identification

A valid photo ID is required at collection so that your sample is matched correctly to your record.

Tell us about medicines

Prescription medicines, supplements and recent procedures can affect how an investigation is scheduled or interpreted — please mention them.

Ask before collection

If anything about preparation is unclear, contact us before your appointment. Preparation errors can affect reporting times.

Patient information

Frequently asked questions

Practical answers about Spinocerebellar Ataxia testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.

How do I choose the right Spinocerebellar Ataxia test?

The correct investigation depends on what your clinician is trying to establish. Review the specimen type and turnaround time below, then confirm the choice with your treating doctor before booking.

What specimen is required?

Specimen requirements are listed for each investigation. If a request involves more than one sample type, our team will confirm what is needed at the time of booking.

Do you offer home sample collection in Dubai and the UAE?

Yes. Home collection can be arranged across Dubai and the wider UAE. Availability and appointment windows vary by location, so please confirm when you book.

How long do results take?

Turnaround depends on the investigation and the method used. The expected reporting time is confirmed with you before collection.

Is there anything I need to do before sample collection?

Some investigations require fasting, a specific collection time, or avoiding certain medicines or activities. Preparation details are shared when you book — please follow them and ask if anything is unclear.

How will I receive my report?

Reports are issued as secure digital documents and can be shared with your referring clinician on request. Please review results with a qualified clinician who can interpret them in context.

About this clinical information

The information on this Spinocerebellar Ataxia page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.

  • Investigation names, specimen types and listed prices are reviewed against laboratory records.
  • Preparation guidance is indicative — confirm test-specific instructions before collection.
  • Content is updated when investigations, methods or reporting formats change.
  • Results are released to the patient and, on request, shared with the referring clinician.

Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.

We're here to help

Need help choosing a Spinocerebellar Ataxia test?

Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.

Call +971 54 548 8731
  • Home collection available across the UAE
  • Digital reports delivered securely
  • Confidential handling of every request

Related areas