12 results
Causes of Pediatric Diarrhea - Differential Diagnosis Algorithm
Infectious:
 • Viral
 • Bacterial
 • Parasitic
Malabsorption:
 • Lactase
Causes of Pediatric ... Differential Diagnosis Algorithm ... Toddler's Diarrhea • Constipation ... #Causes #Peds # ... Pediatrics
Causes of Pediatric Constipation - Differential Diagnosis Algorithm
Dietary / Functional:
 • Insufficient Volume / Bulk
Neurologic:
 •
Causes of Pediatric ... Constipation - ... Differential Diagnosis Algorithm ... #Causes #Peds # ... Pediatrics
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
Pediatric Constipation - Differential Diagnosis Algorithm
Dietary/Functional
 • lnsufficient Volume / Bulk
Neurologic
 • Hirschsprung's Disease
 • Imperforate
Pediatric Constipation ... Differential Diagnosis Algorithm ... #Pediatric #Differential ... #Diagnosis #Algorithm ... #Causes #Peds
Pediatric Dyspnea - Differential Diagnosis Algorithm
Stridor:
 • Croup
 • Foreign Body
 • Tracheitis
 • Epiglottitis
 •
Pediatric Dyspnea ... Differential Diagnosis Algorithm ... Foreign Body Decreased ... #Causes #Peds # ... Pediatrics
Hypochloremia - Differential Diagnosis Algorithm

Cause - Decreased Intake:
 • Low salt in diet
 • Exclusive D5W
Differential Diagnosis Algorithm ... Cause - Decreased ... - Gitelman SIGNS ... acidosis - Cl⁻ decrease ... #Pathophysiology
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Brudzinski’s Sign ... Passive neck flexion causes ... While the pathophysiology ... #PhysicalExam #Pediatrics ... #Peds
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... #Causes #Peds # ... Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
purposes of this algorithm ... lack of tapering, decreased ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki