🇮🇳 NEET PG · subject
NEET PG Paediatrics Syllabus
The Paediatrics syllabus for NEET PG in full: 10 chapters, 38 topics and 85 sub-topics, every one listed below, plus 51 Paediatrics flashcards with answers.
Paediatrics syllabus: all 10 chapters
Expand any chapter to see its topics and sub-topics.
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Normal Growth and Development
3 topics- Growth parameters
- Weight
- Length/Height
- Head circumference
- Growth charts
- Developmental milestones
- Gross motor
- Fine motor
- Language
- Social
- Cognitive development
- Nutritional requirements
- Breastfeeding
- Formula feeding
- Introduction of solid foods
- Nutritional deficiencies
- Growth parameters
-
Neonatology
3 topics- Neonatal resuscitation
- Initial steps
- Positive pressure ventilation
- Chest compressions
- Medications (epinephrine, naloxone)
- Neonatal jaundice
- Physiological jaundice
- Pathological jaundice
- Kernicterus
- Management (phototherapy, exchange transfusion)
- Neonatal infections
- Neonatal sepsis
- Pneumonia
- Meningitis
- Congenital infections (TORCH infections)
- Neonatal resuscitation
-
Infectious Diseases
4 topics- Respiratory infections
- Bronchiolitis
- Pneumonia (viral, bacterial)
- Croup
- Pertussis
- Gastrointestinal infections
- Acute gastroenteritis
- Rotavirus infection
- Hepatitis A
- Typhoid fever
- Central nervous system infections
- Meningitis (bacterial, viral)
- Encephalitis
- Febrile seizures
- Vaccine-preventable diseases
- Diphtheria
- Tetanus
- Pertussis
- Measles
- Mumps
- Rubella
- Polio
- Hepatitis B
- Haemophilus influenzae type b (Hib)
- Pneumococcal disease
- Meningococcal disease
- Varicella
- Influenza
- Human papillomavirus (HPV)
- Respiratory infections
-
Respiratory Disorders
3 topics- Asthma
- Pathophysiology
- Clinical Features
- Diagnosis: Spirometry
- Diagnosis: Peak Flow Meter
- Management: Inhaled Corticosteroids
- Management: Bronchodilators
- Bronchiolitis
- Etiology
- Clinical Features
- Diagnosis
- Management: Supportive Care
- Management: Oxygen Therapy
- Cystic fibrosis
- Pathophysiology
- Clinical Features
- Diagnosis: Sweat Chloride Test
- Management: Airway Clearance Techniques
- Management: Pancreatic Enzyme Replacement
- Asthma
-
Gastroenterology and Nutrition
3 topics- Diarrheal diseases
- Acute diarrhea
- Persistent diarrhea
- Chronic diarrhea: Inflammatory bowel disease
- Chronic diarrhea: Celiac disease
- Gastroesophageal reflux disease (GERD)
- Clinical features
- Diagnosis (pH monitoring)
- Management: Lifestyle modification
- Management: Proton pump inhibitors
- Malnutrition
- Marasmus
- Kwashiorkor
- Vitamin A deficiency
- Iron deficiency anemia
- Nutritional rehabilitation
- Diarrheal diseases
-
Congenital heart diseases
5 topics- Ventricular septal defect (VSD)
- Atrial septal defect (ASD)
- Patent ductus arteriosus (PDA)
- Tetralogy of Fallot
- Coarctation of the aorta
-
Febrile seizures
4 topics- Simple febrile seizures
- Complex febrile seizures
- Risk factors
- Management
-
Acute kidney injury (AKI)
4 topics- Etiology
- Clinical features
- Diagnosis
- Serum creatinine
- Urine output
- Management
-
Type 1 diabetes mellitus
4 topics- Pathophysiology
- Clinical features
- Diagnosis
- Blood glucose
- HbA1c
- Management
- Insulin therapy
- Carbohydrate counting
-
Allergic disorders
5 topics- Allergic rhinitis
- Allergic conjunctivitis
- Atopic dermatitis (eczema)
- Food allergies
- Anaphylaxis
NEET PG Paediatrics flashcards — 51 questions with answers
What is the normal pattern of weight gain in the first year of life relative to birth weight?
Birth weight doubles by ~5 months, triples by 1 year, and quadruples by 2 years. Average newborn loses up to 10% of birth weight in the first week and regains it by 10-14 days. Daily gain is ~25-30 g in the first 3 months.
What is the formula for expected weight (in kg) of a child aged 1-6 years and 7-12 years?
For 1-6 years: weight (kg) = (age in years x 2) + 8. For 7-12 years: weight (kg) = (age in years x 7 - 5) / 2. Useful for quick clinical estimation when scales are unavailable.
How does length/height progress from birth through childhood?
Birth length ~50 cm. It increases by ~25 cm in year 1 (to ~75 cm), ~12 cm in year 2 (to ~87.5 cm), then ~6-8 cm/year until puberty. Length doubles by ~4 years and triples by ~13 years.
What is the expected head circumference at birth and its growth in the first 2 years?
Birth HC ~35 cm. It grows ~2 cm/month for the first 3 months, ~1 cm/month for months 4-6, and ~0.5 cm/month for months 6-12 (total ~12 cm in year 1, reaching ~47 cm). By 2 years HC is ~49 cm; by adulthood ~56-58 cm.
At what ages do the anterior and posterior fontanelles normally close?
The posterior fontanelle closes by 1-2 months. The anterior fontanelle (diamond-shaped) closes between 9 and 18 months. Delayed anterior fontanelle closure suggests hypothyroidism, rickets, raised ICP, or Down syndrome.
List the key gross motor milestones from 3 months to 15 months.
Neck holding ~3 months; sits with support ~5 months; sits without support ~6-8 months; crawls ~9 months; stands with support ~9 months; stands alone ~12 months; walks alone ~12-15 months. Runs by ~18 months.
What are the expected social/adaptive milestones: social smile, stranger anxiety, and waving bye-bye?
Social smile appears by 6-8 weeks. Stranger anxiety develops at ~6-9 months. Waving 'bye-bye' and playing peek-a-boo appear at ~9-10 months. Drinks from a cup by ~12-15 months; feeds self with spoon by ~18 months.
What are the language milestones from cooing to two-word sentences?
Cooing ~2 months; monosyllabic babble ~6 months; bisyllabic babble (mama/dada non-specific) ~9 months; 1-2 words with meaning ~12 months; ~10 words and points to body parts ~18 months; 2-word sentences ~2 years; 3-word sentences ~3 years.
What fine motor/grasp milestones distinguish 4, 6-7, 9, and 12 months?
~4 months: bidextrous (raking) reach/holds objects. ~6-7 months: unidextrous (palmar) grasp, transfers objects. ~9 months: immature pincer grasp. ~12 months: mature pincer grasp; can release voluntarily; makes a tower of 2 cubes by ~15 months.
What are the daily caloric and protein requirements in early infancy versus older children?
Infancy: ~100-110 kcal/kg/day and ~2-2.5 g/kg/day protein. Requirements decline with age: ~90 kcal/kg (1-3 yr), ~70 kcal/kg (4-6 yr). Protein RDA falls to ~1 g/kg/day in older children. Breast milk provides ~67 kcal/100 mL.
When should complementary feeding be started and why not earlier?
Exclusive breastfeeding is recommended for the first 6 months; complementary feeding begins at 6 months because breast milk alone no longer meets energy, iron, and zinc needs. Starting too early risks infection and displaces breast milk; too late risks growth faltering.
What is the recommended sequence of steps in the Neonatal Resuscitation Program (NRP) initial assessment?
At birth ask: term? good tone? breathing/crying? If yes, routine care with mother. If no: provide warmth, position airway, clear secretions if needed, dry, and stimulate (the initial steps within ~30 seconds), then reassess heart rate and respirations.
In neonatal resuscitation, what heart rate threshold triggers positive-pressure ventilation, and what is the next escalation?
If HR < 100/min or apnea/gasping after initial steps, start PPV. If HR remains < 60/min despite 30 seconds of effective PPV (with MR SOPA corrective steps) and an advanced airway, start chest compressions at 3:1 ratio with ventilation, plus 100% oxygen.
What oxygen concentration is recommended for starting resuscitation in term versus preterm neonates?
Term and late-preterm (>= 35 weeks): start with 21% oxygen (room air). Preterm (< 35 weeks): start with 21-30% oxygen, titrated to preductal SpO2 targets. Avoid 100% oxygen initially due to oxidative injury risk.
What is the dose and route of epinephrine in neonatal resuscitation?
Epinephrine 0.01-0.03 mg/kg (0.1-0.3 mL/kg of 1:10,000) IV/umbilical venous, repeated every 3-5 minutes if HR remains < 60/min. Endotracheal dose is higher (0.05-0.1 mg/kg) but IV is preferred.
How do you clinically differentiate physiological from pathological neonatal jaundice?
Physiological jaundice appears after 24 hours, peaks day 3-5 (term), is unconjugated, and resolves by 1-2 weeks. Pathological features: onset < 24 h, total bilirubin rising > 5 mg/dL/day, total > 15 mg/dL, conjugated > 2 mg/dL, or persistence > 2 weeks.
What is kernicterus and which bilirubin component causes it?
Kernicterus is bilirubin-induced neurologic damage from deposition of unconjugated (lipid-soluble, albumin-unbound) bilirubin in the basal ganglia and brainstem. Acute signs: lethargy, hypotonia then hypertonia, retrocollis/opisthotonus; chronic: choreoathetoid CP, gaze palsy, sensorineural deafness.
What is the most common cause of early (<24 h) neonatal jaundice, and how is it managed?
Hemolysis, most commonly Rh or ABO isoimmunization (also G6PD deficiency), causing unconjugated hyperbilirubinemia. Management depends on bilirubin level/age: phototherapy first; exchange transfusion for very high levels or signs of acute bilirubin encephalopathy.
What organisms cause early-onset versus late-onset neonatal sepsis?
Early-onset (<72 h, vertical) is most often Group B Streptococcus and E. coli (in India, Klebsiella, E. coli, and other gram-negatives predominate). Late-onset (>72 h, nosocomial/community) commonly involves coagulase-negative staphylococci, Staph aureus, Klebsiella, and Candida.
What empiric antibiotics are used for neonatal sepsis and what is TORCH?
Empiric therapy is typically ampicillin plus an aminoglycoside (gentamicin), or a cephalosporin if meningitis is suspected, adjusted to local resistance. TORCH = Toxoplasma, Others (syphilis, HIV, parvovirus, VZV), Rubella, CMV, Herpes simplex — congenital infections causing IUGR, rash, and neuro/hepatic involvement.
Show the other 31 Paediatrics flashcards
What clinical sign distinguishes pneumonia from a simple upper respiratory infection in the IMNCI/WHO classification?
Fast breathing (tachypnea) for age defines pneumonia: >= 60/min (<2 months), >= 50/min (2-12 months), >= 40/min (12-59 months). Chest indrawing indicates severe pneumonia; danger signs (cyanosis, inability to feed, convulsions) indicate very severe disease.
What is the most common cause of viral croup and its hallmark features and radiologic sign?
Acute laryngotracheobronchitis (croup) is most often caused by parainfluenza virus. Features: barking/seal-like cough, inspiratory stridor, hoarseness, low-grade fever. X-ray neck shows the subglottic 'steeple sign'. Treat with single-dose dexamethasone; nebulized epinephrine for stridor at rest.
How does acute epiglottitis differ from croup in cause and presentation?
Epiglottitis (classically Haemophilus influenzae type b) presents with acute high fever, drooling, dysphagia, muffled 'hot-potato' voice, tripod posture, and toxic appearance WITHOUT a barking cough. Lateral neck X-ray shows the 'thumbprint sign'. It is an airway emergency — avoid agitating the child.
What are the WHO criteria for assessing dehydration severity in childhood diarrhea?
No dehydration (Plan A): no signs. Some dehydration (Plan B): restless/irritable, sunken eyes, drinks eagerly/thirsty, skin pinch goes back slowly. Severe dehydration (Plan C): lethargic/unconscious, sunken eyes, unable to drink, skin pinch goes back very slowly — needs IV fluids.
What is the composition of low-osmolarity ORS and how is zinc used in diarrhea?
Low-osmolarity ORS (245 mOsm/L): sodium 75, potassium 20, chloride 65, citrate 10, glucose 75 mmol/L. Zinc supplementation (10 mg/day if < 6 months, 20 mg/day if >= 6 months for 14 days) reduces diarrhea duration, severity, and recurrence.
What organism causes acute bacterial meningitis most commonly by age group in children?
Neonates: Group B Strep, E. coli, Listeria. Infants/children (post-neonatal): Streptococcus pneumoniae and Neisseria meningitidis (Hib markedly reduced by vaccination). Empiric therapy: vancomycin + a third-generation cephalosporin (ceftriaxone/cefotaxime); add ampicillin for neonates to cover Listeria.
What CSF findings differentiate bacterial, viral, and tuberculous meningitis?
Bacterial: high neutrophils, glucose low (<40 or CSF:blood <0.4), protein high, turbid. Viral: lymphocytes, normal glucose, mildly raised protein, clear. Tubercular: lymphocytes, very low glucose, very high protein, cobweb clot, raised pressure — subacute course.
List the antigens in the pentavalent vaccine used in India's UIP.
Pentavalent vaccine combines DPT (Diphtheria, Pertussis, Tetanus), Hepatitis B, and Haemophilus influenzae type b (Hib). In India's National Immunization Schedule it is given at 6, 10, and 14 weeks.
What is the Indian National Immunization Schedule at birth and at 6/10/14 weeks?
At birth: BCG, OPV-0, and Hepatitis B birth dose. At 6, 10, and 14 weeks: Pentavalent, OPV, fIPV (inactivated polio), and Rotavirus; PCV is also given (6 & 14 weeks plus booster). Measles/MR is at 9-12 months.
Which vaccines are live-attenuated and what is the key contraindication?
Live vaccines include BCG, OPV, measles/MR/MMR, rotavirus, varicella, and yellow fever. They are contraindicated in significant immunodeficiency and (with caution) pregnancy. Two live parenteral vaccines should be given the same day or separated by >= 4 weeks.
What is the stepwise pharmacologic management of childhood asthma per GINA?
Reliever: as-needed SABA (or low-dose ICS-formoterol). Controllers step up: low-dose ICS, then low-dose ICS + LABA (or medium ICS), then medium/high ICS-LABA, then add-on (LAMA/biologics). Assess control, inhaler technique, and adherence before stepping up.
What clinical and spirometric features support a diagnosis of asthma in a child?
Recurrent wheeze, cough (often nocturnal), breathlessness, and chest tightness, variable and reversible. Spirometry (usually feasible > 5 years) shows obstructive pattern with FEV1/FVC reduced and >= 12% improvement in FEV1 after bronchodilator (reversibility).
What is bronchiolitis: typical age, cause, and management?
Bronchiolitis is a lower-respiratory viral illness in infants < 2 years (peak 2-6 months), most often caused by RSV. Features: coryza progressing to wheeze, fine crackles, respiratory distress, and feeding difficulty. Management is supportive (oxygen, hydration, nasal suction); bronchodilators/steroids are not routinely recommended.
How do you clinically distinguish bronchiolitis from infantile asthma/viral wheeze?
Bronchiolitis: first episode in an infant < 2 years, prodromal coryza, diffuse crackles plus wheeze, RSV season, poor bronchodilator response. Recurrent wheezing episodes, family/personal atopy, and a good bronchodilator response favor asthma/viral-induced wheeze.
What is the genetic basis and inheritance of cystic fibrosis?
Cystic fibrosis is autosomal recessive, caused by mutations in the CFTR gene on chromosome 7 (most common: delta-F508). Defective CFTR chloride channel produces thick secretions affecting lungs, pancreas, intestine, and sweat glands.
What is the diagnostic test for cystic fibrosis and its classic clinical features?
Diagnosis: sweat chloride test (>= 60 mmol/L is positive), supported by genetic testing/newborn screen (raised immunoreactive trypsinogen). Features: recurrent pulmonary infections (Pseudomonas, Staph aureus), pancreatic insufficiency with steatorrhea, failure to thrive, meconium ileus, and male infertility.
What are the WHO classifications of malnutrition (SAM criteria)?
Severe acute malnutrition (SAM): weight-for-height/length < -3 SD, OR MUAC < 11.5 cm (6-59 months), OR bilateral pitting pedal edema. Moderate acute malnutrition: weight-for-height between -2 and -3 SD or MUAC 11.5-12.5 cm.
Compare marasmus and kwashiorkor.
Marasmus: severe wasting from total calorie deficit — marked muscle/fat loss, 'old man' face, weight < 60% expected, NO edema, alert/irritable, appetite preserved. Kwashiorkor: protein deficiency — generalized edema, hepatomegaly (fatty liver), 'flaky paint' dermatosis, hair changes, apathy, anorexia.
What are the steps of WHO management of severe acute malnutrition, including the danger of refeeding?
Stabilization (manage/prevent hypoglycemia, hypothermia, dehydration, infection, electrolyte imbalance, micronutrients) then rehabilitation (catch-up growth with F-100/RUTF). Refeeding too fast causes refeeding syndrome (hypophosphatemia, hypokalemia, hypomagnesemia, cardiac failure) — start cautious feeding with F-75.
What is the most common congenital heart defect, and what murmur does VSD produce?
Ventricular septal defect is the most common congenital heart defect. It causes a left-to-right shunt with a harsh holosystolic (pansystolic) murmur best heard at the left lower sternal border. Large VSDs cause heart failure and may progress to Eisenmenger syndrome.
What are the auscultatory hallmarks of an atrial septal defect?
ASD produces a wide, fixed split S2 (does not vary with respiration) and a mid-systolic ejection murmur at the upper left sternal border (from increased pulmonary flow). Ostium secundum is the most common type; large shunts cause RA/RV enlargement and paradoxical embolism risk.
Describe the murmur and management of patent ductus arteriosus.
PDA causes a continuous 'machinery' murmur at the left infraclavicular/upper left sternal area, wide pulse pressure, and bounding pulses. In preterms, indomethacin or ibuprofen (prostaglandin inhibitors) promote closure; symptomatic/persistent PDAs need catheter device or surgical closure.
What are the four components of Tetralogy of Fallot and its classic X-ray/echo signs?
TOF = (1) VSD, (2) overriding aorta, (3) right ventricular outflow tract obstruction (pulmonary stenosis), (4) right ventricular hypertrophy. Chest X-ray shows a 'boot-shaped' heart (coeur en sabot) with decreased pulmonary vascularity; it is the most common cyanotic CHD beyond infancy.
What is a 'tet spell' and how is it managed acutely?
A hypercyanotic (tet) spell is paroxysmal worsening cyanosis from increased RVOT obstruction/decreased SVR. Management: knee-chest position (increases SVR/venous return), oxygen, morphine, IV fluids, beta-blockers (propranolol/esmolol), and phenylephrine to raise SVR; correct acidosis. Definitive treatment is surgical repair.
What are the clinical features and classic findings of coarctation of the aorta?
Coarctation causes upper-limb hypertension with weak/delayed femoral pulses (radio-femoral delay) and a BP gradient between arms and legs. Chest X-ray shows rib notching (collateral intercostal vessels) and a '3 sign'. Associated with bicuspid aortic valve and Turner syndrome.
Define a simple febrile seizure and its key reassuring features.
A simple febrile seizure is a generalized (tonic-clonic), single seizure lasting < 15 minutes, not recurring within 24 hours, in a child 6 months-5 years with fever and no CNS infection or prior afebrile seizures. It has an excellent prognosis with low epilepsy risk.
What features define a complex febrile seizure?
A complex febrile seizure has any of: focal onset/features, duration > 15 minutes, or recurrence within 24 hours (or within the same febrile illness). Complex features warrant closer evaluation and carry a slightly higher risk of subsequent epilepsy than simple febrile seizures.
What is the management approach to febrile seizures, including when to do a lumbar puncture?
Most febrile seizures are self-limited; treat the fever and reassure, no long-term anticonvulsants for simple cases. Prolonged seizures: benzodiazepines (rectal/IV/buccal). Consider LP if meningeal signs, < 12 months with uncertain status, complex features, or pretreatment with antibiotics masking meningitis.
What is the allergic march and how are allergic rhinitis, conjunctivitis, and atopic dermatitis linked?
The 'atopic march' is the typical progression of IgE-mediated allergic disease: atopic dermatitis (eczema) and food allergy in infancy, followed by allergic rhinitis and asthma in later childhood. Allergic rhinoconjunctivitis (sneezing, itchy nose/eyes, watery rhinorrhea, conjunctival itch/tearing) shares Th2-driven IgE pathophysiology.
Describe atopic dermatitis (eczema) distribution by age and first-line management.
Atopic dermatitis: infancy — face, scalp, extensor surfaces; childhood/adult — flexural creases (antecubital/popliteal fossae). It is intensely pruritic and relapsing, often with raised IgE. Management: liberal emollients (skin barrier), topical corticosteroids for flares, trigger avoidance, and topical calcineurin inhibitors as steroid-sparing agents.
What is anaphylaxis, its most common food triggers in children, and first-line treatment?
Anaphylaxis is a severe, rapid-onset IgE-mediated systemic reaction with airway/breathing/circulation compromise (urticaria, angioedema, wheeze, hypotension, vomiting). Common food triggers: milk, egg, peanut, tree nuts, fish, shellfish. First-line treatment is intramuscular adrenaline 0.01 mg/kg (anterolateral thigh), supine positioning, oxygen, and IV fluids — antihistamines/steroids are adjuncts only.
Same Paediatrics syllabus in other exams
The Paediatrics outline above is identical in these 3 exams:
NEET PG Paediatrics FAQ
What is in the NEET PG Paediatrics syllabus?
NEET PG Paediatrics is split into 10 chapters: Normal Growth and Development, Neonatology, Infectious Diseases, Respiratory Disorders, Gastroenterology and Nutrition, Congenital heart diseases, Febrile seizures, Acute kidney injury (AKI), Type 1 diabetes mellitus and Allergic disorders. Together they contain 38 topics and 85 sub-topics.
How many chapters are in NEET PG Paediatrics?
10 chapters, containing 38 topics and 85 sub-topics. The largest chapter is Congenital heart diseases, with 5 topics.
Are there flashcards for NEET PG Paediatrics?
Yes — a 51-card Paediatrics deck, printed in full in the flashcards section of this page and available in the Examius app with spaced repetition. The free plan covers one exam of your choice, including its flashcards; Examius Pro, a one-time purchase, unlocks every other exam and deck.