Mitochondrial Disorders tests in Dubai & UAE

Compare available Mitochondrial Disorders tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

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1,100.00–4,500.00 AED

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Mitochondrial Disorders test prices

Showing 16–30 of 62 matching tests.

Mitochondrial Disorders diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3682 MitoGenome Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in mitochondrial DNA", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [] Preparation ["Stop heparin medications 48 hours beforehand", "Attend a genetic counselling session for pedigree chart", "No fasting required", "Avoid heparin-containing drugs (including heparin flushes)", "Stay hydrated for easier blood draw"] Indications ["Suspected mitochondrial encephalopathy", "Suspected mitochondrial myopathy", "Suspected multisystem mitochondrial syndromes", "Family history of mitochondrial disorders"] Measurement technique Confirm with laboratory Codes LOINC: 85713-2 ICD-10: E88.4, G71.3 Clinical summary This test analyzes the entire mitochondrial genome to detect pathogenic variants linked to neurological and muscular disorders.
TEST-5104 MPV17 Gene Mitochondrial DNA Depletion Syndrome Type 6 Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MPV17 gene", "SNVs", "Indels", "CNVs"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of all medications"] Indications ["Diagnosis of Mitochondrial DNA Depletion Syndrome Type 6", "Individuals with suggestive clinical features"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: E88.49 Clinical summary This genetic test identifies pathogenic variants in the MPV17 gene associated with Mitochondrial DNA Depletion Syndrome Type 6.
TEST-6140 MRPL44 Gene Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MRPL44 gene", "Mitochondrial function related to MRPL44"] Parameters [] Preparation ["No fasting required", "No medication changes needed", "Inform laboratory of recent blood transfusions"] Indications ["Suspected Combined Oxidative Phosphorylation Deficiency Type 16 (COXPD16)", "Confirmation of clinical diagnosis", "Guidance for metabolic management", "Informed family planning", "Cascade testing in families with known MRPL44 variants"] Measurement technique Confirm with laboratory Codes LOINC: 85872-3 ICD-10: E88.49, G71.3, Z13.79 Clinical summary This test identifies pathogenic variants in the MRPL44 gene associated with Combined Oxidative Phosphorylation Deficiency Type 16 (COXPD16).
TEST-4118 MT-CO1 Gene Cytochrome c Oxidase Subunit I Deficiency Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MT-CO1 gene", "Single-nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy-number changes"] Parameters [] Preparation [] Indications ["Suspected mitochondrial disorder", "Symptoms consistent with cytochrome c oxidase deficiency", "Diagnosis of Leigh syndrome or other mitochondrial encephalomyopathies"] Measurement technique Confirm with laboratory Codes LOINC: 82438-3 ICD-10: E88.42 Clinical summary This test evaluates the MT-CO1 gene for pathogenic variants associated with cytochrome c oxidase deficiency, a mitochondrial disorder.
TEST-5070 MT-CO3 Gene Analysis for Mitochondrial Complex IV Deficiency (NGS) Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MT-CO3 gene sequence", "Pathogenic variants (SNV, indel, CNV)"] Parameters [] Preparation ["No fasting required", "Inform phlebotomy team of all current medications and supplements"] Indications ["Suspected mitochondrial Complex IV deficiency", "Diagnosis of Leigh syndrome", "Diagnosis of mitochondrial encephalomyopathy", "Family history of mitochondrial disorders"] Measurement technique Confirm with laboratory Codes LOINC: 82939-8 ICD-10: E88.40, G31.82, Z13.79 Clinical summary This test evaluates the MT-CO3 gene for pathogenic variants associated with mitochondrial Complex IV deficiency.
TEST-5008 MT-ND1 Gene Mitochondrial Complex I Deficiency Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MT-ND1 gene sequence", "Pathogenic variants", "Heteroplasmy levels"] Parameters [] Preparation ["Do not discontinue prescribed mitochondrial cofactors", "No fasting required"] Indications ["Suspected mitochondrial complex I deficiency", "Diagnosis of Leigh syndrome", "Diagnosis of mitochondrial encephalomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E88.49 Clinical summary This test evaluates the MT-ND1 gene for mutations associated with mitochondrial complex I deficiency.
TEST-5011 MT-ND3 Gene Mitochondrial Complex I Deficiency Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MT-ND3 gene sequence", "Pathogenic variants in MT-ND3"] Parameters [] Preparation ["No specific fasting required", "Inform physician about current anticoagulant therapy"] Indications ["Suspected mitochondrial complex I deficiency", "Family history of mitochondrial disorders", "Carrier screening", "Family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 97405-4 ICD-10: E88.49 Clinical summary This test evaluates the MT-ND3 gene for pathogenic variants associated with mitochondrial complex I deficiency.
TEST-4739 MT-ND3 Gene Sequencing for Leigh Syndrome (Mitochondrial Complex I Deficiency) Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MT-ND3 gene", "Mitochondrial Complex I function (indirectly)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected Leigh syndrome based on clinical presentation", "Family history of mitochondrial disorders", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 53452-5 ICD-10: G31.81 Clinical summary This test identifies pathogenic variants in the MT-ND3 gene, which are linked to Leigh syndrome, a mitochondrial disorder affecting energy production.
TEST-5016 MT-ND4L Gene Mitochondrial Complex I Deficiency Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MT-ND4L gene", "Heteroplasmy levels (variants present in a fraction of mitochondrial DNA)"] Parameters [{"name": "MT-ND4L Gene Sequencing", "reference_range": "No pathogenic variants detected"}, {"name": "Heteroplasmy Level", "reference_range": "Reported as a percentage (%)"}] Preparation ["No specific fasting required", "No medication or diet restrictions unless advised by physician"] Indications ["Patients with clinical features suggestive of mitochondrial complex I deficiency", "Family history of mitochondrial disorders", "Confirmation of suspected diagnosis based on biochemical or neuroimaging findings"] Measurement technique Confirm with laboratory Codes LOINC: 88811-3 ICD-10: E88.89, G31.81 Clinical summary This test evaluates the MT-ND4L gene for pathogenic variants associated with mitochondrial complex I deficiency.
TEST-5122 MT-ND5 Gene Mitochondrial Complex I Deficiency Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MT-ND5 gene variants", "Pathogenic mutations", "Heteroplasmy levels"] Parameters [] Preparation ["No fasting required."] Indications ["Suspected mitochondrial disease", "Diagnosis of Leigh syndrome", "Diagnosis of MELAS", "Evaluation of Complex I deficiency"] Measurement technique Confirm with laboratory Codes LOINC: 101374-8 ICD-10: E88.49 Clinical summary This test analyzes the MT-ND5 gene for mutations associated with mitochondrial Complex I deficiency.
TEST-5020 MT-ND6 Gene Mitochondrial Complex I Deficiency Genetic Test This genetic test evaluates the MT-ND6 gene for pathogenic variants associated with mitochondrial complex I deficiency and related neurological syndromes.	Peripheral Whole Blood (3 mL EDTA) or Dried Blood Spot (FTA Card)	14 to 19 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MT-ND6 gene sequence", "Heteroplasmy levels"] Parameters [] Preparation [] Indications ["Suspected mitochondrial complex I deficiency", "Family history of mitochondrial disease", "Diagnosis of Leigh syndrome, MELAS, or LHON"] Measurement technique Confirm with laboratory Codes LOINC: 82991-0 ICD-10: E88.49 Clinical summary This genetic test evaluates the MT-ND6 gene for pathogenic variants associated with mitochondrial complex I deficiency and related neurological syndromes.
TEST-4172 MT-TA Gene Mitochondrial Myopathy (MT-TA-Related) Genetic Test This test analyzes the entire MT-TA mitochondrial gene for pathogenic variants associated with mitochondrial myopathy, cardiomyopathy, and MELAS spectrum disorders.	Whole Blood, Buccal Swab, or FTA Card	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MT-TA gene sequence", "Copy number variations (CNVs) in MT-TA gene"] Parameters [] Preparation ["No fasting required", "Disclose all supplements, especially CoQ10"] Indications ["Suspected mitochondrial myopathy", "Suspected cardiomyopathy related to MT-TA", "Suspected MELAS spectrum disorder", "Family history of MT-TA related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 104451-2 ICD-10: G71.3 Clinical summary This test analyzes the entire MT-TA mitochondrial gene for pathogenic variants associated with mitochondrial myopathy, cardiomyopathy, and MELAS spectrum disorders.
TEST-4189 MT-TC Gene MELAS Syndrome Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MT-TC gene sequence", "Presence of pathogenic variants"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications"] Indications ["Suspected MELAS syndrome", "Family history of MELAS", "Neurological symptoms suggestive of mitochondrial disease"] Measurement technique Confirm with laboratory Codes LOINC: 94043-5 ICD-10: E88.41 Clinical summary This test evaluates the MT-TC gene for mutations associated with MELAS syndrome.
TEST-4146 MT-TD Gene Analysis for Isolated Mitochondrial Myopathy Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MT-TD gene"] Parameters [] Preparation ["Pre-test genetic counseling is mandatory"] Indications ["Suspected isolated mitochondrial myopathy", "Family history of mitochondrial disorders", "Need for definitive genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81277-9 ICD-10: G71.3 Clinical summary This test detects pathogenic variants in the MT-TD gene associated with isolated mitochondrial myopathy.
TEST-4159 MT-TF Gene MELAS Syndrome Genetic Test 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	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MT-TF gene variants", "Mitochondrial tRNA-Phe gene sequence"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Unexplained stroke-like episodes", "Cardiomyopathy", "Lactic acidosis", "Maternal family history of MELAS"] Measurement technique Confirm with laboratory Codes LOINC: 80872-1 ICD-10: E88.41 Clinical summary This genetic test evaluates the MT-TF gene for variants associated with MELAS syndrome.

Category overview

Mitochondrial Disorders: overview

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.

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