Kerala PSC Previous Years Question Paper & Answer
Page:4
Below are the scanned copy of Kerala Public Service Commission (KPSC) Question Paper with answer keys of Exam Name 'TUTOR TECHNICIAN MEDICAL EDUCATION' And exam conducted in the year 2014. And Question paper code was '028/2014'. Medium of question paper was in Malayalam or English . Booklet Alphacode was 'A'. Answer keys are given at the bottom, but we suggest you to try answering the questions yourself and compare the key along wih to check your performance. Because we would like you to do and practice by yourself.
25.
27,
29.
31.
38.
All are features of hemolytic anaemia except :
(வ Urine urobilinogen absent (B} Hemosiderinuria
)0 Decreased haptoglobin (D) Raised indirect bilirubin
Low serum haptoglobin in hemolysis is masked by :
(A) Pregnancy " (B) Liver disease
(C) Bile duct obstruction (D) Malnutrition
The following protein defects can cause hereditiary spherocytosis except :
(ക) Ankyrin (8) Palladin
(C) Glycophorin C (D) Anion transport protein
Maturation defect in RBC is seenrin :
نف Folic acid and B)2 deficiency (B) Vit. C deficiency
)0( Vit. D deficiency 1) Essential FA deficiency
Osmotic fragility is increased in :
(ಗಿ) Sickle cell anaemia {B) Thalassemia
(0 Hereditary spherocytosis (D) Chronic lead poisoning
The most common cause of AD Hereditary Sphero cytosis is :
(A) mutation in band 3 (ए) mutation in ankyrin
(0) mutation of alpha spectrin (D) mutation of beta spectrin
The most common cause of BETA thalassemia is :
(A) Mutations leading to aberrant slicing (B) Promoter region mutations
(द) Chain terminator mutations (D) Gene mutations
Autoimmune haemolytic anemia is seen in :
(ക ALL (B) AML
(0) ل (D) CML
Which is not seen in Iron deficiency anaemia?
(ക Hyper-segmented neutrophils
{B) Microcytosis preceeds hypochromia
(C) MCHC > 6
(D) Commonest cause of anacmia in India
28/2014 6
