10 results
Validation of the Step-By-Step Approach to Febrile Infants

#Diagnosis #Management #Pediatrics #Peds #Febrile #Infant #StepByStep #Algorithm #LP
Diagnosis #Management #Pediatrics ... #Peds #Febrile ... #Infant #StepByStep ... #Algorithm #LP ... Stratification #Fever
Causes of Pediatric Spells - Differential Diagnosis Algorithm
Neonates and Infant Spells:
 • Benign Sleep Myoclonus
 •
Causes of Pediatric ... Neonates and Infant ... Syndrome Older Infants ... #Causes #Peds # ... Pediatrics
Causes of Acute Pediatric Cough - Differential Diagnosis Algorithm
No Fever, No Tachypnea
 - Normal Chest Auscultation
Causes of Acute ... Pediatric Cough ... Bronchitis - No URTI Symptoms ... #Causes #Peds # ... Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Differential Diagnosis Algorithm ... Sturge-Weber Syndrome Neonates ... #Causes #Peds # ... Pediatrics
Neonatal Infant Pain Scale (NIPS)

For infants less than one year of age, the Neonatal Infant Pain
Neonatal Infant ... Infant Pain Scale ... #Diagnosis #Peds ... #Pediatrics #PainScale ... #Neonatal #Infants
“Step by Step” – the new kid on the block – aims to risk stratify this
“low risk” an infant ... with fever without ... Diagnosis #Management #Pediatrics ... #Peds #Febrile ... #Algorithm #LP
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
depicting the main ... #CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
The Febrile Infant Step-by-Step Algorithm
This is an algorithm developed by European emergency physicians to identify low-risk
The Febrile Infant ... EBM #Management #Pediatrics ... #Peds #Febrile ... #Algorithm #LP ... Stratification #Fever
Childhood Immunization Schedule: Why we immunize
 • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
hemorrhagic rash; symptoms ... non-specific viral symptoms ... jaundice and RUQ pain ... #Immunization #peds ... #pediatrics #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics