1. The first description of sickle cell was in year
2. The disease was named ‘Sickle Cell Anemia’ in the year
3. The yearly world sickle cell day is usually observed/ commemorated on
4 Sickle Cell Awareness month is
5. Sickle Cell Disease is a genetic or hereditary blood disorder of the
6. Mode of Inheritance of Sickle Cell Disease is by
7. Globin Chain production of cells is controlled by gene clusters found on chromosomes
8. If one parent has normal haemoglobin (Hb AA) and the other one has the sickle cell trait (Hb AS), the percentage chance that a pregnancy will result in an offspring with normal haemoglobin (Hb AA) is
9. If one parent has normal haemoglobin (Hb AA) and the other one has the sickle cell trait (Hb AS), the percentage chance that a pregnancy will result in an offspring with the sickle cell Trait (Hb AS) is
10. If one parent has normal haemoglobin (Hb AA) and the other one has the sickle cell trait (Hb AS), the percentage chance that a pregnancy will result in an offspring with the sickle cell anaemia (Hb SS) is
11. If one parent has normal haemoglobin (Hb AA) and the other one has the sickle cell anaemia (Hb SS), the percentage chance that a pregnancy will result in an offspring with normal haemoglobin (Hb AA) is
12. If one parent has normal haemoglobin (Hb AA) and the other one has the sickle cell anaemia (Hb SS), the percentage chance that a pregnancy will result in an offspring with the sickle cell trait (Hb AS).
13. If one parent has normal haemoglobin (Hb AA) and the other one has the sickle cell anaemia (Hb SS), the percentage chance that a pregnancy will result in an offspring with sickle cell anaemia (Hb SS) is
14. If both parents have the sickle cell trait (Hb AS), the percentage chance that a pregnancy will result into an offspring with normal haemoglobin (Hb AA) is
15. If both parents have the sickle cell trait (Hb AS), the percentage chance that a pregnancy will result into an offspring with the sickle cell trait (Hb AS) is
16. If both parents have the sickle cell trait (Hb AS), the percentage chance that a pregnancy will result into an offspring with sickle cell anaemia (Hb SS) is
17. If one parent has the sickle cell trait (Hb AS) and the other one has the sickle cell anaemia (Hb SS), the percentage chance that a pregnancy will result in an offspring with normal haemoglobin (Hb AA) is
18. If one parent has the sickle cell trait (Hb AS) and the other one has the sickle cell anaemia (Hb SS), the percentage chance that a pregnancy will result in an offspring with the sickle cell trait ( Hb AS) is
19. If one parent has the sickle cell trait (Hb AS) and the other one has the sickle cell anaemia (Hb SS ), the percentage chance that a pregnancy will result in an offspring with sickle cell anaemia ( Hb SS) is
20. If both parents have sickle cell anaemia (Hb SS), the percentage chance that a pregnancy will result into an offspring with normal haemoglobin (Hb AA) is
21. If both parents have sickle cell anaemia (Hb SS), the percentage chance that a pregnancy will result into an offspring with the sickle cell trait (Hb AS) is
22. If both parents have sickle cell anaemia (Hb SS), the percentage chance that a pregnancy will result into an offspring with sickle cell anaemia (Hb SS) is
23. The percentage of cases of sickle cell disease that Africa accounts for is
24. The estimated number of infants born with sickle cell anaemia globally each year is
25. The percentage of cases with sickle cell trait (Carrier frequency) across equatorial Africa is
26. The following is NOT a high burden region with SCD in Kenya
27. The following is a high burden region with SCD in Kenya
28. The following is a preliminary test for Sickle Cell Disease
29. The following is a preliminary test for Sickle Cell Disease
30. The following is a screening test for Sickle Cell Disease
31. The following is a Point of Care (POC) test for Sickle Cell Disease
32. The following is a Point of Care (POC) test for Sickle Cell Disease
33. The following is a confirmatory test for Sickle Cell Disease
34. The following is a confirmatory test for Sickle Cell Disease
35. A person who has the sickle cell trait (Hb AS)
36. A person who has the sickle cell anaemia (Hb SS)
37. The TERTIARY interventional strategy in the control of SCD according to the WHO (2006) guidelines entails
38. The SECONDARY interventional strategy in the control of SCD according to the WHO (2006) guidelines entails
39. The PRIMARY interventional strategy in the control of SCD according to the WHO (2006) guidelines entails
40. In sickle cell disease care, prophylactic Pen V should be started at the age
41. The following supplement is recommended in the care of SCD
42. In sickle cell disease care, current recommendations are such that use of Hydroxyurea should be started at age
43. ‘RESPECT OF PERSONS’ is an Ethical Principle in research that deals with
44. ‘BENEFICENCE’ is an Ethical Principle in research that deals with
45. 'JUSTICE’ is an Ethical Principle in research that deals with
46. The study participant/ subject required to sign a ‘CONSENT’ is
47. The study participant/ subject required to sign an ‘ASSENT’ is
48. Which of the following statements is TRUE about the sickle cell disease management situation in Kenya?
49. Which of the following statements is TRUE about the sickle cell disease management situation in Kenya?
50. Which of the following statements is FALSE about the sickle cell disease management situation in Kenya?
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