ratio) due to septal defect, valve lesions, cardiomyopathy
Abdominal X-Ray showing multiple air-fluid level and
dilated colon due to intestinal obstruction
Chest X-Ray showing intestinal coils present in the left
chest causing left lung hypoplasia due to left diaphragmatic hernia. Clinical signs: bowel sounds in left side of the chest, scaphoid abdomen, shifted heart.
Abdominal X-Ray showing double bubble due to duodenal
atresia. Mostly seen in Down syndrome. Treatment: surgical Chest X-Ray showing esophageal atresia with trachea- esophageal fistula hence the air in stomach.
Chest X-Ray showing ground glass appearance and air
bronchogram —> Hyaline membrane disease due to decrease production of surfactant.
Abdominal X-Ray showing air in bowl wall (pneumatosis
intestinalalis) due to necrotizing enterocolitis Chest X-Ray showing jet black area in the right side of the chest with collapsed lung and shift in the mediastinum to the opposite side due to right sided tension pneumothorax. Treatment: intercostal tubal drainage.
Chest X-Ray showing homogenous opacity in the lower
zone of the left lung with centralized mediastinum due to consolidation.
Wrist X-Ray showing cupping and frying of
metaphysical plates of ulna and radius due to rickets. Investigations would show normal to low calcium level, low PO4, high ALP, high PTH, low Fit D (Vit D dependent rickets) Treatment: Vitamin D supplements. Chest X-Ray showing uplifted apex (boot-shaped heart), oligemeic lungs which happen in Tetralogy of Fallot. Complications: Cynotic spell, brain abscess, polycythemia. Characteristic findings on auscultation is an ejection systolic murmur on 2nd intercostal space and soft systolic component of S2
Mangolian spot —> Reassure the parent that it would disappear
with time.
Ruptured meningomyelocele: need surgical correction. May lead
to hydrocephalus.
Neonatal hypotonia —> floppy infant syndrome
Pseudohypertrophy on both calves due to Duchenne muscular dystrophy. X-linked. Investigations: CPK & muscle biopsy
Talipes equinovarus can improve by physiotherapy (if not
bony) or by surgery (if bony)
Hypoglycemic infant (<1.6) due to
familial, diabetic mother, Beckwith Weideman syndrome. May be complicated with: hypoglycemia, respiratory distress, congenital heart disease, transmit hypoparathyroidism
Right sided inguinal hernia (need surgical
correction) & Umblical hernia (can resolve on its own) Pleomorphic skin eruption in chickenpox/Varicella zoster. Complications: varicella encephalitis, cerebral ataxia, pneumonia. Prevention by vaccination. Treatment: supportive ( and Acyclovir for immunocompromised patients)
Cleft & lip palate:
Cause eating problems. May be complicated with ear infection and hearing loss leading to speech delay/problems Require surgical correction
Rocker-bottom foot. Commonly seen in Edward’s
Syndrome (Trisomy 18). Most common heart lesion in this syndrome is Ventricular Septal Defect (VSD).
Baby probably having hydrocephalus. Confirmed
with Brain MRI. Picture showing sun-set appearance of eyes, coverage squint, low set ears, epicanthic fold, depressed nasal bridge. Clubbing and peripheral cyanosis. May be due to cyanotic heart disease, cystic fibrosis, bronchiactasis.
Peeling of skin: late manifestation of Kwasaki disease. Most
serious complication in this disease: coronary artery aneurysms found by serial echocardiogram. Treatment: IV Immunoglobulin (IVIG) & Asprin.
Bilateral foot edema. Common in Turner syndrome
(Monosomy 45 XO). Features: webbing of the neck, wide carrying angle, coarctation of aorta (weak/absent femoral pulse, Hypertension in upper limbs, radio-femoral delay)