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UKMLA Blood & Lymph Practice Questions – Haemoglobinopathies

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x50 Questions. Test your knowledge of haemoglobinopathies with this UKMLA-focused practice question set. Cover important inherited haemoglobin disorders including thalassaemia and clinically relevant haemoglobin variants. Questions explore inheritance, clinical presentations, investigation findings, blood film appearances and key principles of diagnosis and management. Ideal for medical students preparing for UKMLA haematology questions and looking to consolidate high-yield haemoglobinopathy knowledge.

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MLA SB A Qu estion B an k
Haemoglobinopathies
50 single best answer questions — Domain 6: Conditions, Body system: Blood and Lymph




Based on the GMC Medical Licensing Assessment (MLA) content map — applicable from September 2026

,BLOOD AND LY MPH Question 1 of 50

Haemoglobinopathies Sickle-cell crises




A 24-year-old man with known sickle cell disease presents with severe, generalised bone and joint pain that started acutely after a long-
haul flight. He is afebrile with no chest signs. What is the most likely diagnosis?




A Splenic sequestration crisis


B Vaso-occlusive (painful) sickle cell crisis


C Hyperhaemolytic crisis


D Aplastic crisis


E Acute chest syndrome


Select the single best answer.

,BLOOD AND LY MPH Question 1 of 50 — Answer

Haemoglobinopathies Sickle-cell crises




A 24-year-old man with known sickle cell disease presents with severe, generalised bone and joint pain that started acutely after a long-haul flight. He is afebrile with no chest
signs. What is the most likely diagnosis?



A Splenic sequestration crisis


B Vaso-occlusive (painful) sickle cell crisis ✓ Correct



C Hyperhaemolytic crisis


D Aplastic crisis


E Acute chest syndrome



EXPLANATION

Vaso-occlusive crisis, precipitated by triggers such as hypoxia, dehydration, or cold (including on flights), causes severe bone and joint pain due to microvascular
occlusion by sickled red cells.

, BLOOD AND LY MPH Question 2 of 50

Haemoglobinopathies Sickle-cell crises




A 19-year-old woman with sickle cell disease presents with pleuritic chest pain, fever, and a new infiltrate on chest X-ray, alongside falling
oxygen saturations. What is the most likely diagnosis?




A Simple community-acquired pneumonia unrelated to her sickle cell disease


B Pulmonary embolism only


C Aplastic crisis


D Acute chest syndrome


E Vaso-occlusive crisis without pulmonary involvement


Select the single best answer.

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