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Diagnostic options Β· UAE

Hematology tests in Dubai & UAE

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

Tests in this category

114

Listed price range

550.00–7,500.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Hematology test prices

Showing 91–105 of 114 matching tests.

Hematology diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-2882
Pernicious Anemia Panel Test

This diagnostic test evaluates for autoimmune causes of vitamin B12 deficiency by measuring specific antibodies and B12 levels.

Serum (peripheral whole blood) Same-day report (24 hours from morning sample receipt) 1,100.00 AED
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What it measures
["Anti-intrinsic factor antibodies", "Anti-parietal cell antibodies", "Serum vitamin B12 levels"]
Parameters
[{"name": "Anti-Intrinsic Factor Antibody", "reference_range": "Negative"}, {"name": "Anti-Parietal Cell Antibody", "reference_range": "Negative"}, {"name": "Serum Vitamin B12", "reference_range": "null"}]
Preparation
["Overnight fasting (8–12 hours required)", "Water is permitted during fasting"]
Indications
["Suspected pernicious anaemia", "Evaluation of vitamin B12 deficiency", "Differentiation of B12 deficiency causes"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 24322-0 ICD-10: D51.0, E27.4
Clinical summary
This diagnostic test evaluates for autoimmune causes of vitamin B12 deficiency by measuring specific antibodies and B12 levels.
TEST-1228
Plasma Cell Dyscrasia Flow Cytometry Panel (Bone Marrow) Test

This diagnostic test evaluates bone marrow aspirate for the presence and quantity of clonal plasma cells using multicolor flow cytometry.

Bone Marrow Aspirate 1–2 business days 1,800.00 AED
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What it measures
["Clonal plasma cell populations", "Immunophenotype of plasma cells (CD138, CD38, CD45, CD19, CD56, cytoplasmic kappa, cytoplasmic lambda)"]
Parameters
[{"name": "Clonal Plasma Cells", "reference_range": "
Preparation
["No special dietary preparation required.", "Inform clinical team about any anticoagulant or antiplatelet use.", "Valid doctor’s prescription is mandatory."]
Indications
["Suspected multiple myeloma", "Suspected plasmacytoma", "Evaluation of monoclonal gammopathy", "Monitoring response to therapy"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 85327-2 ICD-10: C90.00
Clinical summary
This diagnostic test evaluates bone marrow aspirate for the presence and quantity of clonal plasma cells using multicolor flow cytometry.
TEST-2917
Plasminogen Activator Inhibitor-1 (PAI-1) Test

This diagnostic test evaluates the level of Plasminogen Activator Inhibitor-1 (PAI-1) in platelet-poor plasma, assessing the body's ability to dissolve blood clots.

Platelet-poor plasma 2–3 weeks (sample submission by 7th of month required) 2,500.00 AED
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What it measures
["Plasminogen Activator Inhibitor-1 (PAI-1) antigen", "Fibrinolytic capacity"]
Parameters
[{"name": "PAI-1 Antigen", "reference_range": null}]
Preparation
["12-hour fast required.", "Abstain from smoking and strenuous exercise for 24 hours prior.", "Inform physician about all medications, especially anticoagulants and hormonal therapies.", "Sample collection between 8 AM and 10 AM."]
Indications
["Assessment of risk for venous thromboembolism", "Evaluation of risk for coronary artery disease", "Investigation of recurrent pregnancy loss", "Patients with positive family history of thrombophilia"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 13834-5 ICD-10: D68.6
Clinical summary
This diagnostic test evaluates the level of Plasminogen Activator Inhibitor-1 (PAI-1) in platelet-poor plasma, assessing the body's ability to dissolve blood clots.
TEST-1221
PNH Comprehensive Workup (Flow Cytometry) Test

This diagnostic test evaluates the presence and size of PNH clones by detecting GPI-anchor protein deficiency on blood cells using flow cytometry.

Peripheral whole blood (3 mL EDTA tube) 1–2 calendar days 1,600.00 AED
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What it measures
["Glycosylphosphatidylinositol (GPI)-deficient blood cells", "PNH clone size in granulocytes, monocytes, and red blood cells"]
Parameters
[{"name": "PNH Clone Size (Granulocytes)", "reference_range": "Reported as percentage"}, {"name": "PNH Clone Size (Monocytes)", "reference_range": "Reported as percentage"}, {"name": "PNH Clone Size (Red Blood Cells)", "reference_range": "Reported as percentage"}]
Preparation
["No fasting is required.", "Inform the phlebotomist if you have received a blood transfusion within the past two weeks."]
Indications
["Suspected Paroxysmal Nocturnal Hemoglobinuria (PNH)", "Monitoring PNH clone size", "Guiding treatment decisions for PNH"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 73592-1 ICD-10: D59.5, D61.09, D64.9
Clinical summary
This diagnostic test evaluates the presence and size of PNH clones by detecting GPI-anchor protein deficiency on blood cells using flow cytometry.
TEST-1201
Prenatal Alpha Thalassemia Mutation Screening (3 Common Mutations) Test

This test identifies the presence or absence of three common alpha-globin gene deletions (--⁠SEA, -α3.7, -α4.2) in fetal DNA.

Fetal genomic DNA (Amniotic fluid, Chorionic villi, Cord blood) 10–12 Working Days 1,000.00 AED
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What it measures
["Alpha-globin gene deletions (--⁠SEA, -α3.7, -α4.2)", "Carrier status for alpha-thalassemia"]
Parameters
[]
Preparation
["No specific patient preparation required for the test itself.", "Consult managing obstetrician or genetic counselor regarding medication or supplement continuation."]
Indications
["At-risk couples planning a pregnancy", "Early gestation screening for alpha-thalassemia"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21671-8 ICD-10: Z13.0
Clinical summary
This test identifies the presence or absence of three common alpha-globin gene deletions (--⁠SEA, -α3.7, -α4.2) in fetal DNA.
TEST-1652
Prenatal Delta Beta-Thalassemia Mutation Screening Test

This test detects specific large deletions in the HBB gene cluster associated with delta-beta thalassemia using End Point PCR.

Amniotic fluid, Chorionic villi, or Peripheral blood 5–6 calendar days 1,000.00 AED
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What it measures
["HBB gene cluster deletions", "Delta-beta thalassemia mutations"]
Parameters
[]
Preparation
[]
Indications
["Prenatal diagnosis of delta-beta thalassemia", "Carrier screening for delta-beta thalassemia", "Reproductive planning", "Differentiation from other thalassemia syndromes"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21637-2 ICD-10: D56.8
Clinical summary
This test detects specific large deletions in the HBB gene cluster associated with delta-beta thalassemia using End Point PCR.
TEST-2979
Protein C Antigen Test

This test measures the quantity of Protein C antigen in the blood to help diagnose deficiencies and assess the risk of blood clots.

Whole Blood 2–3 weeks 2,500.00 AED
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What it measures
["Protein C antigen levels", "Natural anticoagulant activity"]
Parameters
[{"name": "Protein C Antigen", "reference_range": null}]
Preparation
["No specific fasting required", "Do not suspend anticoagulant medication without clinician instruction"]
Indications
["Diagnosis of hereditary or acquired Protein C deficiency", "Assessment of thrombotic risk", "Evaluation after unexplained VTE"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 27815-8 ICD-10: D68.59
Clinical summary
This test measures the quantity of Protein C antigen in the blood to help diagnose deficiencies and assess the risk of blood clots.
TEST-2998
Protein C Functional Test

This test evaluates the functional activity of Protein C, a key natural anticoagulant protein in the blood.

Platelet-poor plasma Same day (sample received by 11 AM) 800.00 AED
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What it measures
["Protein C enzymatic activity", "Anticoagulant function"]
Parameters
[{"name": "Protein C Functional Activity", "reference_range": null}]
Preparation
["Overnight fasting is preferred.", "Heparin must be paused for 1 day and oral anticoagulants for 7 days, only with physician’s prior consent."]
Indications
["Evaluation of thrombophilia", "Diagnosis of hereditary or acquired Protein C deficiency", "Risk assessment for VTE"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 21192-5 ICD-10: D68.59
Clinical summary
This test evaluates the functional activity of Protein C, a key natural anticoagulant protein in the blood.
TEST-2995
PROTEIN S ACTIVITY (FUNCTIONAL) Test

This diagnostic test evaluates the functional activity level of Protein S, a natural anticoagulant, to assess the risk of blood clot formation.

Peripheral whole blood (citrated) 24–48 hours 800.00 AED
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What it measures
["Functional activity of Protein S", "Enzymatic function of Protein S"]
Parameters
[{"name": "Protein S Activity", "reference_range": null}]
Preparation
["Fast overnight", "Temporarily discontinue anticoagulants under physician guidance"]
Indications
["Evaluation of inherited thrombophilia", "Evaluation of acquired thrombophilia", "Risk assessment for venous thromboembolism (VTE)"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 5959-0 ICD-10: D68.59
Clinical summary
This diagnostic test evaluates the functional activity level of Protein S, a natural anticoagulant, to assess the risk of blood clot formation.
TEST-2961
Protein S Antigen Free Test

This diagnostic test evaluates the level of free, functional protein S in the blood.

Whole Blood (3 mL, sodium citrate) Same day (sample received by 11 AM) 1,200.00 AED
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What it measures
["Free Protein S Antigen", "Natural Anticoagulant Activity"]
Parameters
[{"name": "Free Protein S Antigen", "reference_range": null}]
Preparation
["Overnight fasting preferred", "Temporary cessation of Heparin (1 day) and Oral Anticoagulants (7 days) prior to sampling, with physician consent"]
Indications
["Suspected hereditary protein S deficiency", "Suspected acquired protein S deficiency", "Evaluation of thrombophilia risk"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 57029-3 ICD-10: D68.5
Clinical summary
This diagnostic test evaluates the level of free, functional protein S in the blood.
TEST-2965
Protein S Antigen Total Test

This test measures the total amount of Protein S in the blood to help identify potential deficiencies linked to an increased risk of blood clots.

Platelet-poor plasma (PPP) 14–21 calendar days 2,800.00 AED
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What it measures
["Total circulating Protein S concentration", "Natural anticoagulant levels"]
Parameters
[{"name": "Protein S Antigen Total", "reference_range": null}]
Preparation
["Overnight fasting (8–12 hours) is recommended.", "Complete Coagulation Requisition Form (Form 15) and Test Send-Out Consent Form (Form 35)."]
Indications
["Screening for inherited or acquired Protein S deficiency", "Evaluation of thrombophilia risk", "Pre-operative assessment for major surgery", "Assessment before long-term anticoagulation"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 12072-5 ICD-10: D68.59
Clinical summary
This test measures the total amount of Protein S in the blood to help identify potential deficiencies linked to an increased risk of blood clots.
TEST-3376
Serum Viscosity Test

This diagnostic test evaluates the thickness or resistance to flow of serum, primarily to screen for hyperviscosity syndrome.

Serum 2–3 weeks post-monthly batch cut-off 1,500.00 AED
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What it measures
["Blood fluid resistance", "Serum viscosity"]
Parameters
[{"name": "Serum Viscosity", "reference_range": "WHO-recognised hyperviscosity thresholds (e.g., >3.5 centipoise)"}]
Preparation
["Fasting for 8–10 hours is advised", "Continue all medications unless your doctor specifies otherwise"]
Indications
["Screening for hyperviscosity syndrome", "Monitoring WaldenstrΓΆm macroglobulinemia", "Monitoring multiple myeloma", "Evaluation of suspected plasma cell disorders"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 3012-5 ICD-10: R70.1
Clinical summary
This diagnostic test evaluates the thickness or resistance to flow of serum, primarily to screen for hyperviscosity syndrome.
TEST-3263
Thalassemia Monitoring Panel Test

This diagnostic test evaluates key blood parameters, including complete blood count, iron stores, hemolysis markers, and hemoglobin fractions, to monitor thalassemia patients.

Peripheral whole blood, serum, or plasma Within 24 hours (Daily) 750.00 AED
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What it measures
["Complete blood count (CBC)", "Iron stores (ferritin)", "Hemolysis markers (LDH, bilirubin)", "Hemoglobin fractions (HbA2)"]
Parameters
[{"name": "Complete Blood Count (CBC)", "reference_range": null}, {"name": "Ferritin", "reference_range": null}, {"name": "LDH (Lactate Dehydrogenase)", "reference_range": null}, {"name": "Bilirubin", "reference_range": null}, {"name": "Hemoglobin Fractions (HbA2)", "reference_range": null}]
Preparation
["An 8-hour fasting is mandatory", "Do not discontinue prescribed medication (e.g., iron chelators, folic acid) without consulting your doctor"]
Indications
["Monitoring transfusion dependence in thalassemia patients", "Assessing iron overload status", "Evaluating hemolysis", "Guiding chelation therapy"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 24336-0 ICD-10: D56.1
Clinical summary
This diagnostic test evaluates key blood parameters, including complete blood count, iron stores, hemolysis markers, and hemoglobin fractions, to monitor thalassemia patients.
TEST-3281
Thrombophilia Comprehensive Profile Test

This test evaluates inherited and acquired factors contributing to an increased risk of blood clot formation (thrombophilia). It combines genetic mutation analysis with functional...

Whole blood (serum and plasma) 2–3 working days from batch (Sample Mon/Thu by 11 AM) 2,800.00 AED
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What it measures
["Factor V Leiden mutation", "Prothrombin G20210A mutation", "MTHFR variants", "Protein C activity", "Protein S free antigen", "Antithrombin activity", "Lupus anticoagulant screen"]
Parameters
[{"name": "Factor V Leiden", "reference_range": null}, {"name": "Prothrombin G20210A", "reference_range": null}, {"name": "MTHFR variants", "reference_range": null}, {"name": "Protein C activity", "reference_range": null}, {"name": "Protein S free antigen", "reference_range": null}, {"name": "Antithrombin activity", "reference_range": null}, {"name": "Lupus anticoagulant screen", "reference_range": null}]
Preparation
["Fasting for 8–12 hours is recommended", "Discontinue Heparin 24 hours prior", "Discontinue oral anticoagulants (warfarin, apixaban, rivaroxaban) 7 days prior under physician supervision", "Do not stop any medication without doctor's approval"]
Indications
["Evaluation of unexplained venous thromboembolism", "Assessment of risk in patients with a family history of thrombophilia", "Investigation of recurrent pregnancy loss", "Pre-operative risk assessment in certain cases"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 51915-3 ICD-10: D68.5, D68.6, Z13.0
Clinical summary
This test evaluates inherited and acquired factors contributing to an increased risk of blood clot formation (thrombophilia). It combines genetic mutation analysis with functional protein activity and antigen level measurements.
TEST-1378
Thrombophilia Genetic Panel (MTHFR, Factor V Leiden, Prothrombin G20210A) Test

This genetic panel evaluates for three specific inherited mutations associated with an increased risk of blood clot formation.

Peripheral whole blood 3–4 days 1,600.00 AED
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What it measures
["MTHFR C677T gene mutation", "Factor V Leiden (G1691A) gene mutation", "Prothrombin G20210A gene mutation"]
Parameters
[{"name": "MTHFR C677T", "reference_range": "Homozygous Wild-Type (CC), Heterozygous (CT), Homozygous Mutant (TT)"}, {"name": "Factor V Leiden (G1691A)", "reference_range": "Homozygous Wild-Type (GG), Heterozygous (GA), Homozygous Mutant (AA)"}, {"name": "Prothrombin G20210A", "reference_range": "Homozygous Wild-Type (GG), Heterozygous (GA), Homozygous Mutant (AA)"}]
Preparation
["No fasting required", "Hydrate well", "Bring doctor's prescription or valid ID for home collection"]
Indications
["Personal or family history of venous thromboembolism", "Evaluation before major surgery", "Investigation of recurrent pregnancy loss", "Assessment of risk in specific medical conditions"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 24331-0 ICD-10: Z13.79
Clinical summary
This genetic panel evaluates for three specific inherited mutations associated with an increased risk of blood clot formation.

Category overview

Hematology: overview

When it comes to your circulatory health, finding precise and timely answers is essential for your peace of mind and ongoing vitality. The Hematology department at DNA Labs UAE uses highly advanced flow cytometry and automated cell counters to thoroughly analyze your blood profile. From routine counts to specialized coagulation and hematology testing in the UAE, these diagnostics provide your doctor with crucial data to manage and monitor blood-related conditions effectively. Trust in one of the most reliable diagnostic labs in Dubai and the UAE to deliver fast, highly accurate results under uncompromising confidentiality standards. Ensure your circulatory wellness today. View our hematology tests, arrange a convenient home collection, or contact our medical experts to schedule your visit.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.

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