- (A) Thrombocytopenia
- (B) Von Willebrand disease
- (C) Hemophilia
- (D) Ehlers danlos syndrome
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- (A) immature neutrophils
- (B) erythrocytes
- (C) matures neutrophils
- (D) Platelets
- (A) jaundice
- (B) Kernicterus
- (C) Haemosiderosis
- (D) All of the above
- (A) Hemophilia A is due to deficiency of factor VIII
- (B) In hemophilia A females are carriers
- (C) Desmopressin is useful in the management of hemophilia A
- (D) Levels of factor VIII less than 50% are associated with spontaneous hemorrhage
- (A) Acute myeloid leukemia
- (B) Chronic monocytic leukemia
- (C) Chronic lymphoblastic leukemia
- (D) Chronic myeloid leukemia
- (A) Ferritin
- (B) Haemosiderin
- (C) Myoglobin
- (D) Transferrin
- (A) Classic hemophilia
- (B) Christmas disease
- (C) Vitamin K deficiency
- (D) Idiopathic thrombocytopenic purpura
- (A) Hemophilia
- (B) Hemolytic anaemia
- (C) Aplastic anaemia
- (D) Megaloblastic anemia
- (A) African jaw lymphoma
- (B) Hodgkin’s disease
- (C) Burkitt’s lymphoma
- (D) Infectious mononucleosis
- (A) Increased bleeding time and clotting time
- (B) Decreased bleeding time and clotting time
- (C) Decreased bleeding time and increased clotting time
- (D) Normal bleeding time and increased clotting time
