Some of the AIIMS June 2020 Paediatrics questions as recalled by students
(These are recall based questions and hence the options and reconstruction of questions may slightly vary from original questions)
((Disclaimer - Subjected to Memory bias - ☺))
Q1. Hand to hand shift development in a
6 months old baby, what does it
indicate?
a. Visual motor coordination
b. Voluntary release
c. Hand brain coordination
d. Release phenomenon
explaination -Reference Nelson Page 132
Q2.Vitamin deficiency causing neonatal
seizure:
a. Pyridoxine
b. Pantothenic acid
c. Biotin
d. Thiamine
explaination -Pyridoxine dependency and
pyridoxal -5 phosphate dependency
causes neonatal seizures
Q3. Correction of VSD is done to avoid
or correct:
a. Failure to thrive
b. Arrythmia
c. Heart attack
d. Respiratory alkalosis
explaination -Indications for surgical closure of VSD
a. Patient at any age with large defects in
whom clinical symptoms and failure to
thrive cannot be controlled medically.
b. Infant between 6 and 12 months of
age with moderate to large defect
associated with pulmonary
hypertension even if the symptoms
are controlled by medication.
c. Patient older than 24 months with Qp
: Qs ratio greater than 2 : 1
d. Supracristal VSD
Q4. All are true in a severe acute
malnutrition except:
a. Weight for age less than 3 SD
b. Weight for height less than
3SD
c. Oedema
d. Mid arm circumference less
than 110 mm
explaination -Diagnosis of SAM
a. Weight for height <70% of
expected or < - 3Z score
b. Mid upper arm circumference
< 11.5 cm
c. Edema
Q5. In phototherapy bilirubin is
converted to:
a. Lumirubin
b. Biliverdin
explaination -In phototherapy –
• Structural isomerisation
o Bilirubin is converted to
lumirubin
Photo isomerisation
o 4Z, 15Z – bilirubin is
converted to 4Z, 15E – bilirubin
Q6. 2 months back history of fever with
bloody diarrhoea in a child followed
by swollen, red and errythematous
joint:
a. Rota virus
b. Shigella
c. E. Coli
d. Giordia
explaination -Post infectious complication in entric
infections
a. Reactive arthritis
i. Salmonella
ii. Shigella
iii. Yersinia
iv. Campylobacter
b. Guillain – Barre syndrome
i. Campylobacter
c. Haemolytic uremic syndrome –
i. STEC
ii. Shigella dysentenae 1
Q7. Features of severe dehydration
except:
a. Thirsty child
b. Sunken fontanelle
c. Skin pitch return slowly
d. Drowsy
Q8. All are indicative of paediatric
asthma except:
a. Increase in FEV1 > 12% after
bronchodilator
b. AM : PM variation > 15%
c. FEV1 decrease more than
15% after exercise
d. FEV1 / FVC < 80%
explaination - Lung Function Abnormalities in Asthma and Assessment of
Airway Inflammation
• Spirometry (in clinic)
• Airflow limitation:
o Low FEV1 (relative to percentage of predicted
norms)
o FEV1/FVC ratio <0.80
• Bronchodilator response (to inhaled β-agonist) assesses
reversibility of airflow limitation.
• Reversibility is determined by an increase in either
FEV1>1 2% or predicted FEV1)10% after inhalation of a
short-acting
• B-agonist (SABA)
• Exercise challenge:
o Worsening in FEV1 ≥ 15%
• Daily peak expiratory flow (PEF) or FEV1 monitoring:
day-to-day and / or AM-to-PM variation ≥20%
Q9. Osteomalacia is developed due to
excess excretion of phosphate in
urine. What is the diagnosis:
a. Antiepileptic drug
b. Vit D resistance
c. Hereditary
d. Vit D deficiency
explaination -Among the genetic disorders causing
rickets
X linked hypophosphatemic is the
most common
Increased fibroblast excretion
Overproduction of FGF23 is also seen
in –
a. Tumour induced osteomalacia
b. McCune Albright syndrome
c. Fanconisyndrome
d. Dent disease
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