Genetics
Mitochondrial Disorders 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.
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Mitochondrial Disorders investigations
All 62 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| ATP5F1A Gene Sequencing for Mitochondrial Complex V Deficiency, Nuclear Type 4 (NGS) Test TEST-5083 LOINC 94891-5 | This test evaluates the ATP5F1A gene for mutations associated with mitochondrial complex V deficiency, nuclear type 4. | Peripheral whole blood (EDTA) or buccal swab | 3–4 weeks | 2,800.00 AED | Details |
| ATP5F1E Gene Test TEST-5182 LOINC 93495-7 | This diagnostic test evaluates the ATP5F1E gene for pathogenic variants associated with Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear Typ... | Whole Blood (EDTA Tube), Extracted DNA (≥1 µg), or Dried Blood Spot on FTA Card | 3 to 4 Weeks | 2,800.00 AED | Details |
| COX15 Gene Leigh Syndrome Genetic Test TEST-4622 LOINC 21677-0 | This diagnostic test evaluates the entire coding region of the COX15 gene for pathogenic variants associated with Leigh syndrome. | Whole Blood (Peripheral) or FTA Card | 3 to 4 Weeks | 2,800.00 AED | Details |
| FARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 14 Genetic Test TEST-6136 LOINC 81247-9 | This genetic test evaluates the FARS2 gene for variants associated with Combined Oxidative Phosphorylation Deficiency Type 14 (COXPD14), a rare mitoch... | Whole blood (EDTA, 3–5 mL), Extracted DNA (≥1 µg, 260/280 1.8–2.0), or one-drop blood on FTA card | 3–4 weeks | 2,800.00 AED | Details |
| FASTKD2 Gene Test TEST-5172 LOINC 94222-3 | This test detects pathogenic variants in the FASTKD2 gene, which are associated with Mitochondrial Complex IV Deficiency. | Whole Blood, Extracted DNA, or One-drop Blood on FTA Card | 3 – 4 Weeks | 2,800.00 AED | Details |
| FOXRED1 Gene Genetic Test TEST-5110 LOINC 98569-1 | This genetic test analyzes the FOXRED1 gene to detect variants associated with mitochondrial complex I deficiency and Leigh syndrome. | Peripheral Blood (Whole Blood) in EDTA | 3–4 weeks | 2,800.00 AED | Details |
| GTPBP3 Gene Combined Oxidative Phosphorylation Deficiency Type 23 Test TEST-6156 LOINC 103318-6 | This test evaluates the entire coding region of the GTPBP3 gene for pathogenic variants associated with Combined Oxidative Phosphorylation Deficiency... | Whole blood or buccal swab | 3–4 Weeks (expedited available) | 2,800.00 AED | Details |
| IBA57 Gene (Multiple Mitochondrial Dysfunctions Syndrome Type 3) Genetic Test TEST-5138 LOINC 101847-9 | This genetic test analyzes the IBA57 gene to detect mutations causing Multiple Mitochondrial Dysfunctions Syndrome Type 3. | Peripheral Whole Blood (EDTA) | 3–4 Weeks | 2,800.00 AED | Details |
| ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 (MMDS4) Genetic Test TEST-5237 LOINC 101804-6 | This genetic test identifies pathogenic variants, including point mutations and copy number variations, within the ISCA2 gene associated with Multiple... | Whole Blood / Extracted DNA / FTA Card | 3 to 4 Weeks | 2,800.00 AED | Details |
| Leber’s Hereditary Optic Neuropathy (LHON) Mitochondrial Mutation Detection Test TEST-2358 LOINC 94087-3 | This test detects specific pathogenic point mutations in mitochondrial DNA associated with Leber’s Hereditary Optic Neuropathy (LHON). It confirms the... | Whole blood (4 mL EDTA, lavender-top tube) | 4 weeks | 3,500.00 AED | Details |
| Leigh Syndrome Mitochondrial Mutation Detection Test TEST-2385 LOINC 93360-1 | This test identifies pathogenic variants within the entire mitochondrial DNA (mtDNA) associated with Leigh syndrome. | Whole blood | Report by Friday if sample received by Monday 9 AM | 1,200.00 AED | Details |
| MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes) Mutation Detection Test TEST-2565 LOINC 58221-6 | This test detects the specific m.3243A>G mutation in the MTTL1 gene, the most common cause of MELAS syndrome. | Whole Blood (EDTA) | 5 working days (Sunday–Thursday) | 1,100.00 AED | Details |
| MFF Gene Mitochondrial Encephalomyopathy Genetic Test TEST-5209 LOINC 62896-9 | This genetic test evaluates the MFF gene for pathogenic variants associated with mitochondrial encephalomyopathy, a progressive neurological disorder. | Whole Blood, Extracted DNA, or FTA Card (One Drop Blood) | 3 to 4 Weeks | 2,800.00 AED | Details |
| Mitochondrial Genome Sequencing and Analysis Test TEST-283 LOINC 64518-6 | This test evaluates the entire mitochondrial genome for mutations and variations. | Whole Blood or Extracted DNA | 8 Weeks | 3,500.00 AED | Details |
| Mitochondrial Mutation Detection Comprehensive Panel Test TEST-2554 LOINC 101376-0 | This test evaluates the entire mitochondrial DNA and over 300 nuclear genes associated with mitochondrial disease. | Peripheral whole blood (4 mL lavender-top EDTA tube) | 5 working days | 4,500.00 AED | Details |
| MitoGenome Genetic Test TEST-3682 LOINC 85713-2 | This test analyzes the entire mitochondrial genome to detect pathogenic variants linked to neurological and muscular disorders. | Whole blood (EDTA lavender-top or citrate blue-top) | 3–4 weeks | 3,000.00 AED | Details |
| MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test TEST-5104 LOINC 82939-0 | This genetic test identifies pathogenic variants in the MPV17 gene associated with Mitochondrial DNA Depletion Syndrome Type 6. | Peripheral Blood or DNA FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| MRPL44 Gene Test TEST-6140 LOINC 85872-3 | This test identifies pathogenic variants in the MRPL44 gene associated with Combined Oxidative Phosphorylation Deficiency Type 16 (COXPD16). | Peripheral Whole Blood (EDTA) | 3–4 Weeks | 2,800.00 AED | Details |
| MT-CO1 Gene Cytochrome c Oxidase Subunit I Deficiency Genetic Test TEST-4118 LOINC 82438-3 | This test evaluates the MT-CO1 gene for pathogenic variants associated with cytochrome c oxidase deficiency, a mitochondrial disorder. | Whole blood (EDTA) | 3–4 weeks from sample receipt | 2,800.00 AED | Details |
| MT-CO3 Gene Analysis for Mitochondrial Complex IV Deficiency (NGS) Test TEST-5070 LOINC 82939-8 | This test evaluates the MT-CO3 gene for pathogenic variants associated with mitochondrial Complex IV deficiency. | Whole Blood (EDTA), Extracted DNA, or FTA Card Specimen | 3–4 Weeks | 2,800.00 AED | Details |
| MT-ND1 Gene Mitochondrial Complex I Deficiency Genetic Test TEST-5008 LOINC 81247-9 | This test evaluates the MT-ND1 gene for mutations associated with mitochondrial complex I deficiency. | Peripheral whole blood (3–5 mL EDTA) or FTA card (dried blood spot) | 3–4 Weeks | 2,800.00 AED | Details |
| MT-ND3 Gene Mitochondrial Complex I Deficiency Genetic Test TEST-5011 LOINC 97405-4 | This test evaluates the MT-ND3 gene for pathogenic variants associated with mitochondrial complex I deficiency. | Peripheral Whole Blood (EDTA), Extracted DNA, or FTA Card | 3 to 4 weeks | 2,800.00 AED | Details |
| MT-ND3 Gene Sequencing for Leigh Syndrome (Mitochondrial Complex I Deficiency) Test TEST-4739 LOINC 53452-5 | This test identifies pathogenic variants in the MT-ND3 gene, which are linked to Leigh syndrome, a mitochondrial disorder affecting energy production. | Peripheral Whole Blood (EDTA) or Extracted DNA (FTA Card) | 3–4 Weeks | 2,800.00 AED | Details |
| MT-ND4L Gene Mitochondrial Complex I Deficiency Genetic Test TEST-5016 LOINC 88811-3 | This test evaluates the MT-ND4L gene for pathogenic variants associated with mitochondrial complex I deficiency. | Whole Blood (Peripheral) or FTA Card | 3-4 Weeks | 2,800.00 AED | Details |
| MT-ND5 Gene Mitochondrial Complex I Deficiency Genetic Test TEST-5122 LOINC 101374-8 | This test analyzes the MT-ND5 gene for mutations associated with mitochondrial Complex I deficiency. | Whole Blood (EDTA), Extracted DNA, or FTA Card | 21–28 calendar days | 2,800.00 AED | Details |
| MT-ND6 Gene Mitochondrial Complex I Deficiency Genetic Test TEST-5020 LOINC 82991-0 | This genetic test evaluates the MT-ND6 gene for pathogenic variants associated with mitochondrial complex I deficiency and related neurological syndro... | Peripheral Whole Blood (3 mL EDTA) or Dried Blood Spot (FTA Card) | 14 to 19 Business Days | 2,800.00 AED | Details |
| MT-TA Gene Mitochondrial Myopathy (MT-TA-Related) Genetic Test TEST-4172 LOINC 104451-2 | This test analyzes the entire MT-TA mitochondrial gene for pathogenic variants associated with mitochondrial myopathy, cardiomyopathy, and MELAS spect... | Whole Blood, Buccal Swab, or FTA Card | 3 – 4 weeks | 2,800.00 AED | Details |
| MT-TC Gene MELAS Syndrome Genetic Test TEST-4189 LOINC 94043-5 | This test evaluates the MT-TC gene for mutations associated with MELAS syndrome. | Whole Blood EDTA or Buccal Swab | 3 to 4 weeks | 2,800.00 AED | Details |
| MT-TD Gene Analysis for Isolated Mitochondrial Myopathy Test TEST-4146 LOINC 81277-9 | This test detects pathogenic variants in the MT-TD gene associated with isolated mitochondrial myopathy. | Peripheral Whole Blood, DNA FTA Card, or Extracted DNA | 3–4 weeks | 2,800.00 AED | Details |
| MT-TF Gene MELAS Syndrome Genetic Test TEST-4159 LOINC 80872-1 | This genetic test evaluates the MT-TF gene for variants associated with MELAS syndrome. | Peripheral Whole Blood (EDTA) | 3–4 Weeks | 2,800.00 AED | Details |
| MT-TL1 Gene Genetic Testing for MELAS Syndrome Test TEST-6057 LOINC 81303-2 | This diagnostic test evaluates the MT-TL1 mitochondrial gene for mutations associated with MELAS syndrome. | Peripheral Whole Blood | 3–4 Weeks | 2,800.00 AED | Details |
| MT-TL1 Gene MELAS Syndrome Genetic Test TEST-4186 LOINC 81209-0 | This diagnostic test evaluates the MT-TL1 gene for mutations associated with MELAS syndrome. | Peripheral whole blood (EDTA) or buccal swab | 3–4 weeks | 2,800.00 AED | Details |
| MT-TN Gene Sequencing for Mitochondrial Complex I Deficiency (Genetic Test) TEST-5048 LOINC 81286-7 | This genetic test identifies pathogenic variants in the MT-TN gene, which are associated with mitochondrial complex I deficiency and related neurometa... | Peripheral Whole Blood (3–5 mL in EDTA tube) | 3–4 weeks (21–28 calendar days) | 2,800.00 AED | Details |
| MT-TP Gene (MERRF Syndrome) Genetic Test TEST-4783 LOINC 81247-9 | This genetic test detects pathogenic variants in the MT-TP gene, which encodes mitochondrial tRNA for proline, associated with MERRF syndrome. | EDTA Whole Blood (Peripheral Blood, 5 mL) | 3–4 weeks from sample receipt | 2,800.00 AED | Details |
| MT-TQ Gene Myopathy Genetic Test TEST-4133 LOINC 85439-0 | This test identifies pathogenic mutations in the mitochondrial MT-TQ gene associated with myopathy and neurological disorders. | Peripheral whole blood (two EDTA tubes, 5 mL each), extracted DNA, or FTA card | 21–28 calendar days | 2,800.00 AED | Details |
| MT-TR Mitochondrial Encephalomyopathy Genetic Test (NGS) TEST-4368 LOINC 101234-5 | This test identifies pathogenic variants in the MT-TR gene associated with mitochondrial encephalomyopathy. | Whole Blood (2–3 mL) | 3 to 4 weeks | 2,800.00 AED | Details |
| MT-TS1 Genetic Test for MERRF/MELAS Overlap Syndrome TEST-4984 LOINC 86247-0 | This test detects pathogenic variants in the MT-TS1 gene associated with MERRF/MELAS overlap syndrome. | Whole Blood (Peripheral) | 3 to 4 Weeks | 2,800.00 AED | Details |
| MT‑TK Gene MERRF Syndrome (MT‑TK Related) Genetic Test TEST-4980 LOINC 81304-1 | This test evaluates the MT-TK gene for pathogenic variants associated with Myoclonic Epilepsy with Ragged-Red Fibers (MERRF) syndrome. | Peripheral Whole Blood (EDTA) or FTA Card Finger-Prick | 3–4 Weeks | 2,800.00 AED | Details |
| MT‑TL1 Gene MELAS Syndrome Genetic Test TEST-4772 LOINC 81247-7 | This test provides a definitive molecular diagnosis for MELAS syndrome by sequencing the entire MT‑TL1 gene. | Peripheral Whole Blood (3‑5 mL in EDTA tube) or Dried Blood Spot (FTA card) | 3-4 Weeks | 2,800.00 AED | Details |
| MT‑TM Gene‑Related Mitochondrial Myopathy NGS Test TEST-4142 LOINC 81313-5 | This test sequences the entire MT‑TM gene to detect pathogenic variants associated with mitochondrial myopathy. | Peripheral whole blood, extracted DNA, or FTA card specimen | 3–4 weeks from sample receipt | 2,800.00 AED | Details |
| MT‑TV Gene (Leigh Syndrome) Genetic Test TEST-5399 LOINC 101350-8 | This test detects pathogenic variants in the MT-TV gene associated with Leigh Syndrome using Next-Generation Sequencing. | Whole Blood (EDTA), Buccal Swab, or Extracted DNA | 14 – 21 Business Days | 2,800.00 AED | Details |
| MTFMT Gene Combined Oxidative Phosphorylation Deficiency Type 15 Genetic Test TEST-6236 LOINC 21636-6 | This test identifies pathogenic variants in the MTFMT gene associated with combined oxidative phosphorylation deficiency type 15. | Peripheral Whole Blood or Extracted DNA | 3-4 Weeks | 2,800.00 AED | Details |
| NARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 24 Genetic Test TEST-6253 LOINC 86211-9 | This genetic test identifies mutations in the NARS2 gene associated with Combined Oxidative Phosphorylation Deficiency Type 24 (COXPD24). | Whole blood (EDTA, 3–5 mL), extracted DNA (>2 µg), or dried blood spot (FTA card) | 3–4 weeks (urgent option: 14 days) | 2,800.00 AED | Details |
| NDUFA11 Gene Mitochondrial Complex I Deficiency Next-Generation Sequencing (NGS) Genetic Test TEST-5024 LOINC 94219-6 | This test identifies pathogenic variants in the NDUFA11 gene associated with mitochondrial complex I deficiency. | Peripheral Whole Blood, Extracted DNA, or Dried Blood Spot (FTA Card) | 3 to 4 Weeks | 2,800.00 AED | Details |
| NDUFAF1 Gene Mitochondrial Complex I Deficiency Genetic Test TEST-5128 LOINC 92931-7 | This test evaluates the NDUFAF1 gene for pathogenic variants associated with mitochondrial complex I deficiency. | Peripheral whole blood (or FTA card / extracted DNA) | 3–4 Weeks | 2,800.00 AED | Details |
| NDUFAF3 Gene Mitochondrial Complex I Deficiency NGS Test TEST-5026 LOINC 94041-6 | This test identifies pathogenic variants in the NDUFAF3 gene associated with mitochondrial Complex I deficiency. | Peripheral whole blood | 3–4 weeks (expedited reporting available for critically ill neonates and urgent clinical indications) | 2,800.00 AED | Details |
| NDUFAF4 Gene Mitochondrial Complex I Deficiency Genetic Test TEST-5133 LOINC 21636-6 | This test identifies pathogenic variants in the NDUFAF4 gene associated with Mitochondrial Complex I Deficiency. | Peripheral Blood (3-5 mL EDTA) or Saliva (Oragene OG-500 kit) | 3 to 4 weeks | 2,800.00 AED | Details |
| NDUFS6 Gene (Mitochondrial Complex I Deficiency) Genetic Test TEST-5144 LOINC 94228-7 | This genetic test identifies pathogenic variants in the NDUFS6 gene, which are responsible for mitochondrial complex I deficiency, a severe neurometab... | Whole Blood (Peripheral Blood) – EDTA tube | 3–4 weeks | 2,800.00 AED | Details |
| NDUFV2 Gene Mitochondrial Complex I Deficiency Genetic Test TEST-5150 LOINC 82173-6 | This genetic test identifies mutations in the NDUFV2 gene associated with mitochondrial complex I deficiency. | Whole Blood (EDTA) or Dried Blood Spot (FTA Card) | 3–4 Weeks | 2,800.00 AED | Details |
| NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 (MMDS1) Genetic Test TEST-5134 LOINC 82319-8 | This test identifies pathogenic variants in the NFU1 gene associated with Multiple Mitochondrial Dysfunctions Syndrome Type 1 (MMDS1). | Whole Blood (3-5 ml) or Dried Blood Spot (FTA Card) | 3-4 Weeks (expedited upon request) | 2,800.00 AED | Details |
| POLG Gene Mitochondrial DNA Depletion Syndrome Type 4A Genetic Test TEST-5099 LOINC 101308-6 | This genetic test evaluates the POLG gene for pathogenic variants associated with mitochondrial DNA depletion syndrome type 4A (Alpers-Huttenlocher sy... | Peripheral Whole Blood, DNA FTA Card, or Extracted DNA | 3–4 Weeks | 2,800.00 AED | Details |
| POLG Gene Mitochondrial DNA Depletion Syndrome Type 4B Genetic Test TEST-5201 LOINC 94862-4 | This diagnostic test evaluates the entire coding region of the POLG gene for variants associated with Mitochondrial DNA Depletion Syndrome Type 4B (MT... | Peripheral Whole Blood (EDTA) or FTA Card | 3–4 weeks | 2,800.00 AED | Details |
| RNASEH1 Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 2 Genetic Test TEST-5619 LOINC 93569-1 | This genetic test identifies mutations in the RNASEH1 gene associated with autosomal recessive progressive external ophthalmoplegia with mitochondrial... | Whole Blood | 3–4 weeks | 2,800.00 AED | Details |
| RRM2B Gene (PEOA5) Genetic Test TEST-5542 LOINC 84496-8 | This genetic test identifies dominant mutations in the RRM2B gene associated with progressive external ophthalmoplegia with mitochondrial DNA deletion... | Whole blood (peripheral), dried blood spot on FTA card, or extracted DNA | 3 – 4 Weeks | 2,800.00 AED | Details |
| SDHD Gene Mitochondrial Complex II Deficiency NGS Genetic Analysis Test TEST-5053 LOINC 21642-3 | This test evaluates the SDHD gene for pathogenic variants associated with mitochondrial complex II deficiency and hereditary paraganglioma-pheochromoc... | Whole blood (EDTA), extracted DNA (≥1 µg), or dried blood spot (FTA card) | 3–4 Weeks | 2,800.00 AED | Details |
| SUCLA2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test TEST-5188 LOINC 21730-8 | This genetic test analyzes the SUCLA2 gene for pathogenic variants associated with mitochondrial DNA depletion syndrome type 5 (MTDPS5). | Whole Blood (EDTA), Extracted DNA, or FTA Card | 3 to 4 Weeks | 2,800.00 AED | Details |
| SUCLG1 Gene Genetic Test for Mitochondrial DNA Depletion Syndrome (Encephalomyopathic Type with Methylmalonic Aciduria) TEST-5109 LOINC 94233-3 | This test identifies pathogenic variants in the SUCLG1 gene associated with a specific type of mitochondrial DNA depletion syndrome. | Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card) | 3–4 Weeks | 2,800.00 AED | Details |
| TMEM70 Gene Analysis (Mitochondrial Complex V Deficiency, Nuclear Type 2) Test TEST-5077 LOINC 81337-8 | This genetic test analyzes the TMEM70 gene to detect pathogenic variants associated with Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear Ty... | Whole Blood (EDTA), Extracted DNA, or FTA Card (blood spot) | 3 to 4 weeks from sample receipt | 2,800.00 AED | Details |
| TWNK (C10orf2) Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 3 Autosomal Dominant Genetic Test TEST-5537 LOINC 81247-9 | This genetic test analyzes the TWNK gene to detect mutations associated with Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 3... | Whole blood (EDTA), extracted DNA, or FTA card | 3–4 weeks | 2,800.00 AED | Details |
| TWNK Gene MTDPS7 Genetic Test TEST-5206 LOINC 81247-9 | This test identifies pathogenic variants in the TWNK gene associated with mitochondrial DNA depletion syndrome type 7 (MTDPS7). | Whole Blood (EDTA), FTA Card, or Extracted Genomic DNA | 3–4 weeks | 2,800.00 AED | Details |
| UQCC2 Gene (Mitochondrial Complex III Deficiency, Nuclear Type 7) Genetic Test TEST-5065 LOINC 48776-7 | This genetic test identifies pathogenic variants in the UQCC2 gene associated with mitochondrial complex III deficiency, nuclear type 7. | Whole blood, extracted DNA, or FTA card | 3–4 Weeks | 2,800.00 AED | Details |
| UQCRQ Gene Mitochondrial Complex III Deficiency Genetic Test TEST-5061 LOINC 48018-6 | This test identifies pathogenic variants in the UQCRQ gene associated with mitochondrial complex III deficiency. | Peripheral whole blood (venipuncture) | 3 to 4 weeks | 2,800.00 AED | Details |
Clinical overview
About Mitochondrial Disorders
Complex, overlapping symptoms that dramatically worsen with illness or metabolic stress often trace back to hidden hereditary defects in cellular energy production, demanding rigorous molecular oversight. Integrated into our elite Genetics and Metabolic services, comprehensive testing for Mitochondrial Disorders maps the intricate genetic pathways governing your mitochondria to pinpoint exactly where energy production fails. Utilizing advanced genomic profiling, this expansive screening uncovers the biological root of systemic fatigue and organ dysfunction, safely guiding your healthcare provider in tailoring highly personalized supportive therapies, customized nutritional interventions, and proactive preventative care. Trusted for clinical excellence among top diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, uncompromising diagnostic precision, and remarkably fast reporting. Take an empowered step toward targeted wellness—book your mitochondrial disorders testing in UAE, arrange a secure clinical sample collection, or connect with our specialized medical experts today.
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 Mitochondrial Disorders testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.
How do I choose the right Mitochondrial Disorders 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 Mitochondrial Disorders 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.
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