24 results
Common pediatric rashes you see in clinic. How to differentiate them? Name that rash.

#pediatrics #peds #rashes
Common pediatric ... How to differentiate ... #pediatrics #peds ... #rashes #clinical ... #comparison #table
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... the lab values table ... Diagnosis #Algorithm #Differential ... #Neonatology #Peds ... #Pediatrics #Table
Web chart of etiologies related to inflammatory head and neck masses.

#pediatrics #peds #differential #causes #pearls #head
#pediatrics #peds ... #differential # ... causes #pearls # ... head #neck #masses ... viral #bacterial #clinical
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
Metabolism A table ... from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table
Epiglottitis - Swollen inflamed epiglottis 
Clinical (Rapid onset) 
 • Fever 
 • Sore throat
inflamed epiglottis Clinical ... Epiglottitis #Signs #Causes ... #Diagnosis #Differential ... #Peds #Pediatrics
Paradoxical Breathing on Physical Exam

Paradoxical breathing is often a sign of breathing problems. It causes the
It causes the chest ... #respiratory #clinical ... #video #pulmonary ... #peds #pediatrics
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
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... Video by Dr. ... Sign #Meningitis #Clinical ... #Pediatrics #Peds
Landau's Reaction (Reflex)  on Physical Exam

Landau's reaction is investigated holding the baby firmly under the
child will be able ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics