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

#Diagnosis #Management #Pediatrics #Peds #Febrile #Infant #StepByStep #Algorithm #LP
Approach to Febrile Infants ... Management #Pediatrics #Peds ... #Febrile #Infant ... #StepByStep #Algorithm ... #LP #Antibiotics
Causes of Pediatric Spells - Differential Diagnosis Algorithm
Neonates and Infant Spells:
 • Benign Sleep Myoclonus
 •
Differential Diagnosis Algorithm ... Neonates and Infant ... Syndrome Older Infants ... Spells: • Breath-holding ... #Causes #Peds #
“Step by Step” – the new kid on the block – aims to risk stratify this
“low risk” an infant ... Management #Pediatrics #Peds ... #Febrile #Infant ... #StepByStep #Algorithm ... #LP #Antibiotics
gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... #Infant #Diabetic ... OBGYN #Diagnosis #Pathophysiology ... Complications #Peds
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Differential Diagnosis Algorithm ... Focal Epilepsy of Infancy ... Spells: • Breath-holding ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Algorithm for the evaluation of the crying infant #Diagnosis #EM #Peds #Crying #Infant #Algorithm
Algorithm for the ... evaluation of the crying ... infant #Diagnosis ... #EM #Peds #Crying ... #Infant #Algorithm
The Febrile Infant Step-by-Step Algorithm
This is an algorithm developed by European emergency physicians to identify low-risk
The Febrile Infant ... Step-by-Step Algorithm ... This is an algorithm ... Management #Pediatrics #Peds ... #LP #Antibiotics
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Differential Diagnosis Algorithm ... Hernia Witnessed Choking ... Breathing • Apnea of Infancy ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... deficiencies present in infants ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds