14 results
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Seizures - Differential ... #Epilepsy #Differential ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Causes of Unprovoked Pediatric Seizures -  Epilepsy Syndromes - Differential Diagnosis Algorithm 
Infantile:
 • Benign
Causes of Unprovoked ... Pediatric Seizures ... Infancy • West ... #Differential # ... #Peds #Pediatrics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... ) - Differential ... Neurologic: • Seizure ... Infancy #LifeThreatening ... #Peds #Pediatrics
Causes of Severe Aortic Regurgitation - Differential Diagnosis
Acute:
 • Leaflet: Traumatic Rupture, Acute Infective Endocarditis, Acute
Causes of Severe ... Valvuoplasty • Aorta ... Dysfunction Chronic - Aorta ... : • Infxn + Inflammatory ... #cardiology
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
tachypnea or wheeze - Clinical ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant ... Tachypnea #Wheeze #Differential
Aortic Dissection Pearls
Aortic dissection is caused by a tear in the tunica intima, the innermost layer
is caused by a ... aorta. ... • FHx of aortic ... Examine for: • Pulse ... deficit/differential
Tetralogy of Falot on Chest X-Ray
Tetralogy of Falot comprises four defects -
1. Ventricular septal defect (VSD)
2.
Overriding aorta ... boot shaped heart caused ... Chest #XRay #CXR #clinical ... #radiology #peds ... #pediatrics #cardiology
Figure of 3 Sign - Coarctation of the Aorta on Chest X-Ray

The figure of 3 sign
the Aorta on Chest ... the aorta. ... the aorta. ... is not seen in infancy ... #radiology #pediatrics
Newborn Infant - Routine Examination

Birthweight, gestational age and birthweight percentile are noted.
General observation Of the baby's
The femoral pulses ... Their pulse pressure ... the aorta. ... #Examination #Peds ... #Pediatrics #Diagnosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... deficiencies present in infants ... endocrinology #peds ... #pediatrics