Related Questions

The following enzyme deficiencies lead to hemolytic anemia
A Pyruvate kinase
B Glucose 6 phosphate dehydrogenase
C Lactate dehydrogenase
D Pyruvate dehydrogenase complex
E NADPH Oxidase
Hereditary hemolytic anemia is
A Thalassemia
B Aplastic anemia
C Megaloblastic anemia
D Leukemia
Laboratory features present in hemolytic jaundice are
A Raised serum bilirubin
B Increased urobilinogen in urine
C High serum alkaline phosphatase [Davidson's/P-852]
D Presence of bilirubin in urine
E Decreased stercobilinogen in stool
Diagnosis of hemolytic uremic syndrome is based on the following feature/s
A Azotemia
B Thrombocytopenia
C Increased LDH
D Hematuria
E Neutropenia
Following enzyme deficiency leads to hemolytic anaemia
A Pyruvate kinase
B Glucose 6-phosphate dehydrogenase
C Lactate dehydrogenase
D Pyruvate dehydrogenase complex
E NADPH oxidase
Features of anemia of chronic disease are
A Low reticulocyte count
B Raised hepcidin level
C Normal or low ferritin
D High total iron binding capacity
E High soluble transferrin receptor
Usual laboratory features of iron deficiency anemia are
A ↓Serum ferritin
B ↑Total iron binding capacity
C ↓Transferring saturation
D ↑Serum transferrin
E ↑Serum ceruloplasmin
A 25-year-old woman with 30-week-pregnancy developed pallor and her blood report shows Hb-7.5 gm/dl, MCV 65 fl, MCH 18 pg. For further evaluation of her anemia, required investigations include
A Serum ferritin
B Serum iron
C Total iron binding capacity
D Soluble transferrin receptor assay
E Serum protein electrophoresis
A 60 year old gentleman has been diagnosed as vitamin B12 deficiency due to pernicious anemia . which o the following is unlikely to happen?
A Posterioor column involvement
B Optic atrophy
C Corticospina tract involvement
D Seizure
Microcytic hypochrmic anemia is found in:
A Thalassaemia
B Multiple myeloma
C Liver disease
D Infective endocarditis

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