DHA Hematology Laboratory exam questions
Blood cells, haemostasis, haemoglobinopathies, blood bank and QC.
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DHA Hematology Laboratory exam at a glance
- Exam code
- MTH4612
- Questions
- 150 MCQs
- Duration
- 3 hours
- Pass mark
- 55%
- Fee per attempt
- USD 240 (about AED 880)
- Result
- Pass or fail, no score
From the DHA CBT Guideline, Sep 2026. Delivered by Prometric; three attempts in total across the UAE authorities. Full DHA exam guide.
Try two questions from this bank
Original questions from the bank - pick an answer to see the rationale and reference.
A blood film from a patient who had a splenectomy after trauma shows small, round, dense purple inclusions in many red cells. What are these inclusions?
Choose an answer to see the rationale.
Rod-shaped azurophilic cytoplasmic inclusions are seen in blasts on a peripheral film. What do they indicate?
Choose an answer to see the rationale.
Not sure where you stand? Sit 12 of these questions free, timed at real exam pace, and see which domains you are weakest in.
Take the free mock exam →Liked those? The full bank has 450 questions at this standard - every one with a rationale and a reference.
Get the full bank - AED 249What's inside
- ✓3 full-length papers (~150 Q each)
- ✓450 questions, no overlap between papers
- ✓Four options, one unambiguous best answer
- ✓A full rationale on every question
- ✓A real guideline or textbook reference
- ✓Every sub-topic in the published blueprint
The Hematology Laboratory exam in every GCC country
| Regulator | Exam | Format | Pass mark | Fee per attempt | Practise |
|---|---|---|---|---|---|
| DHA Dubai | Hematology Technologist (MTH4612) | 150 MCQs in 3 hours | 55% | USD 240 (about AED 880) | DHA questions → |
| DOH Abu Dhabi, Al Ain and Al Dhafra | DOH licensing exam Regulator-wide format | Written + oral/OSCE | Pass / fail only | Not published | DOH questions → |
| MOHAP Northern Emirates - Ajman, Umm Al Quwain, Ras Al Khaimah and Fujairah | MOHAP licensing exam Regulator-wide format | Computer-based | Not published | Not published | MOHAP questions → |
| SHA Emirate of Sharjah | SHA licensing exam Regulator-wide format | Set at assessment | Not published | Not published | SHA questions → |
| SCFHS Kingdom of Saudi Arabia | SCFHS licensing exam Regulator-wide format | 200 MCQs, 240 min | 500-560 of 800 | Not published | SCFHS questions → |
| QCHP State of Qatar | QCHP licensing exam Regulator-wide format | 150 MCQs, 3 hrs | 50-65% | Not published | QCHP questions → |
| NHRA Kingdom of Bahrain | NHRA licensing exam Regulator-wide format | Prometric CBT | Not published | Not published | NHRA questions → |
| OMSB Sultanate of Oman | OMSB licensing exam Regulator-wide format | Computer-based OC exam | Not published | Not published | OMSB questions → |
| Kuwait MOH State of Kuwait | Kuwait MOH licensing exam Regulator-wide format | 150 MCQs, 170 min | 60-70% | Not published | Kuwait MOH questions → |
exact exam published for Hematology Laboratory
From each regulator's own exam pages; anything a regulator does not publish says so. Assessment mode also depends on your licence title, so confirm your route on your eligibility notice.
Try 15 free Hematology Laboratory questions with answersDifferent from the samples on this page - each with a full explanationStart →What the Hematology Laboratory exam covers
The published blueprint for this exam breaks into 8 domains and 50 testable sub-topics. Our bank covers every one of them - here is the full map, so you can see exactly what you are expected to know.
Haematopoiesis and Blood Cell Morphology~12%6 topics
- Haematopoiesis and cell maturation sequences
- Red cell morphology: poikilocytes and their causes
- Red cell inclusions: Howell-Jolly, Pappenheimer, Heinz, basophilic stippling
- White cell morphology: toxic changes, Auer rods, smudge cells
- Platelet morphology and estimation from the film
- Romanowsky staining and film preparation
Red Cell Disorders and Anaemia~18%7 topics
- Red cell indices: calculation and interpretation
- Iron deficiency and anaemia of inflammation
- Megaloblastic anaemia: B12 and folate
- Hereditary spherocytosis and membrane disorders
- G6PD and pyruvate kinase deficiency
- Immune haemolysis and the direct antiglobulin test
- Cold agglutinins and analyser artefacts
Haemoglobinopathies and Thalassaemias~10%6 topics
- Beta-thalassaemia trait and HbA2 quantitation
- Alpha-thalassaemia and HbH inclusions
- Sickle cell disease: solubility test and HPLC
- Discriminant indices: Mentzer index
- HPLC and capillary electrophoresis interpretation
- Premarital and neonatal haemoglobinopathy screening
White Cell Disorders and Haematological Malignancy~15%7 topics
- Absolute counts and reactive changes
- Acute myeloid leukaemia including APL
- Acute lymphoblastic leukaemia
- Chronic myeloid leukaemia and BCR-ABL1
- Chronic lymphocytic leukaemia and lymphoma immunophenotyping
- Myeloproliferative neoplasms and myelodysplasia
- Cytochemistry: MPO, Sudan black, NSE
Haemostasis and Coagulation~18%8 topics
- Coagulation sample requirements: citrate ratio and fill volume
- PT, INR and APTT principles
- Mixing studies: factor deficiency versus inhibitor
- Lupus anticoagulant testing
- Heparin and anticoagulant monitoring: anti-Xa
- Von Willebrand disease testing
- Fibrinogen, D-dimer and DIC
- Platelet function testing
Automation, Flow Cytometry and Quality Control~12%6 topics
- Impedance and optical cell counting principles
- Analyser flags and spurious results
- Pseudothrombocytopenia and platelet clumping
- Nucleated red cell correction of WBC
- Internal QC: Levey-Jennings charts and Westgard rules
- External quality assessment and method verification
Specimen Handling, Laboratory Safety and Ethics~8%5 topics
- Patient identification and sample labelling
- Order of draw and anticoagulants
- Sample stability and storage
- Biosafety: spills, centrifuge breakage, PPE
- Critical result reporting and confidentiality
Special Haematology Tests~7%5 topics
- Erythrocyte sedimentation rate methods
- Reticulocyte counting
- PNH testing by flow cytometry
- Bone marrow aspirate and trephine processing
- Body fluid cell counts
6 worked Hematology Laboratory practice questions
Original exam-style questions from the bank, spread across the blueprint domains. They are not real or recalled exam questions. Try each one, then open the answer for the rationale and reference. None of them appear in the free mock exam, so reading them will not spoil it.
Question 1 · Automation, Flow Cytometry and Quality Control
An analyser reports a WBC of 12.0 x 10^9/L on a sample in which 20 nucleated red cells are counted per 100 white cells. What is the corrected WBC count?
- A9.6 x 10^9/L
- B14.4 x 10^9/L
- C10.0 x 10^9/L
- D11.8 x 10^9/L
Show answer and explanation
Correct answer: C. 10.0 x 10^9/L
Corrected WBC = WBC x 100 / (100 + NRBC) = 12.0 x 100 / 120 = 10.0 x 10^9/L. Subtracting 20% of the count (giving 9.6) uses the wrong denominator.
Reference: Dacie and Lewis Practical Haematology, 12th ed.
Question 2 · Haematopoiesis and Blood Cell Morphology
A 70-year-old has a lymphocytosis of 28 x 10^9/L with many small mature lymphocytes and numerous smudge cells on the film. Which diagnosis is most likely?
- AAcute lymphoblastic leukaemia
- BInfectious mononucleosis
- CHairy cell leukaemia
- DChronic lymphocytic leukaemia
Show answer and explanation
Correct answer: D. Chronic lymphocytic leukaemia
Smudge cells are fragile lymphocytes damaged during film spreading and are characteristic of CLL with a mature small lymphocytosis. Infectious mononucleosis shows large reactive lymphocytes rather than uniform small cells.
Reference: Bain BJ. Blood Cells: A Practical Guide, 6th ed.
Question 3 · Haemostasis and Coagulation
For routine PT and APTT testing, what blood-to-anticoagulant ratio is required in a 3.2% sodium citrate tube?
- A4:1
- B9:1
- C1:1
- D20:1
Show answer and explanation
Correct answer: B. 9:1
Coagulation tubes require a 9:1 ratio of blood to 3.2% sodium citrate, and should be filled to at least 90% of the nominal volume. A 4:1 ratio is used for Westergren ESR tubes.
Reference: CLSI H21-A5: Collection, Transport and Processing of Blood Specimens for Coagulation Testing
Question 4 · Haemostasis and Coagulation
A patient with mild bleeding and thrombocytopenia shows platelet aggregation at a low ristocetin concentration that does not aggregate normal platelets. Which condition is suggested?
- AType 1 von Willebrand disease
- BBernard-Soulier syndrome
- CGlanzmann thrombasthenia
- DType 2B von Willebrand disease
Show answer and explanation
Correct answer: D. Type 2B von Willebrand disease
Enhanced ristocetin-induced platelet aggregation at low ristocetin concentration reflects increased affinity of VWF for platelet GPIb, characteristic of type 2B VWD (or platelet-type VWD). Bernard-Soulier syndrome shows absent ristocetin aggregation.
Reference: ASH/ISTH/NHF/WFH Guidelines on the Diagnosis of von Willebrand Disease 2021
Question 5 · Red Cell Disorders and Anaemia
An analyser reports RBC 1.9 x 10^12/L, Hb 110 g/L, MCV 118 fL and MCHC 420 g/L, and the film shows red cell clumps. What is the most appropriate action?
- AReport the results with a comment
- BWarm the sample to 37 C and re-run
- CRequest a new sample in citrate
- DDilute the sample with water
Show answer and explanation
Correct answer: B. Warm the sample to 37 C and re-run
Cold agglutinins clump red cells so that doublets are counted as single large cells, falsely lowering the RBC and raising MCV and MCHC; warming to 37 C disperses them. A new citrate sample does not prevent cold agglutination, and water would lyse the cells.
Reference: Dacie and Lewis Practical Haematology, 12th ed.
Question 6 · Red Cell Disorders and Anaemia
A child has spherocytes, a negative direct antiglobulin test and a family history of anaemia and gallstones. Which laboratory test is recommended for screening hereditary spherocytosis?
- AOsmotic fragility on fresh blood only
- BHb electrophoresis
- CEosin-5-maleimide (EMA) binding test
- DSickle solubility test
Show answer and explanation
Correct answer: C. Eosin-5-maleimide (EMA) binding test
The EMA binding test by flow cytometry measures reduced band 3-related membrane proteins and is a sensitive, specific screening test for hereditary spherocytosis. Haemoglobin electrophoresis assesses haemoglobin variants, not membrane defects.
Reference: BSH Guidelines for the Diagnosis and Management of Hereditary Spherocytosis 2011
Last reviewed September 2026
About these questions: every question is original, written to the published blueprint, with a rationale and a reference. No recalled or leaked exam content is used. How we write our questions.
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