14 results
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
algorithm #causes #pediatrics ... CongenitalAdrenalHyperplasia #diagnosis ... #comparison #treatment ... #Peds #Endocrinology ... #Adrenal #pathophysiology
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 ... #Neonatology #Peds ... #Pediatrics #Table
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
Metabolism A table ... additions, for diagnosing ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table
Tetralogy of Fallot Summary
 • Anatomy
 • Incidence
 • Pathophysiology
 • Presentation
 • Common Variants
 •
• Incidence • Pathophysiology ... Tetralogy #Fallot #diagnosis ... management #cardiology #peds ... #pediatrics #treatment
Pediatric SVT - Management Algorithm
Identify SVT:
 • HR not variable
 • Abrupt rate changes
 • Infants:
Pediatric SVT - ... variable • Abrupt rate ... AP Stable? ... Management #Algorithm #peds ... #Pediatric #treatment
Salter Harris Fractures - Pediatric Fractures of the Physis 
SALTR Mnemonic 

Salter Harris I 
Straight through
epiphysis, the growth plate ... ortho treatment ... ortho treatment ... #Peds #Orthopedics ... #Diagnosis #Management
IDSA 2017 CDiff Guidelines - Table 2. Recommendations for the Treatment of Clostridium difficile Infection in Children

#Management
CDiff Guidelines - Table ... Recommendations for the Treatment ... of Clostridium difficile ... #Management #Peds ... #Pediatrics #Clostridium
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
- Differential Diagnosis ... Short Stature (Late ... Panhypopituitarism Treatment ... #Algorithm #endocrinology ... #causes #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
, vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
1995) CRIES (Table ... been validated to date ... #Diagnosis #Peds ... #Pediatrics #PainScale