21 results
Step by Step Algorithmic Approach to Pediatric Fever

Age < 21 days old (or 28 days for
Algorithmic Approach to Pediatric ... Leukocytes in the urine ... #Peds #Diagnosis ... #Management #StepByStep ... #Algorithm #Infant
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... loss Reduced urine ... Extremities #PhysicalExam ... #Dehydration #Peds ... #Pediatrics
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children

Urinary
Clinical Algorithm ... Evaluation and Management ... UTI #Algorithm #Diagnosis ... #Management #Febrile ... #Infant #Peds #
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
this video, the infant ... Sign #Meningitis #Clinical ... #Video #PhysicalExam ... #Pediatrics #Peds ... #neurology
“Step by Step” – the new kid on the block – aims to risk stratify this
“low risk” an infant ... leukocytes in urine ... CRP < 20 mg/L #Diagnosis ... #Management #Pediatrics ... #Peds #Febrile
Pyloric Stenosis - Overview - Lightning Learning

Thickened pyloric muscle obstructing the passage of milk going into
Incidence: 2-4 infants ... Cause is unknown ... Pyloric #Stenosis #Diagnosis ... #Management #Pediatrics ... #Peds
Infant UTI Algorithm (<8 weeks of age)

Emergency Medicine Cases @EMCases

#Infant #Pediatric #UTI #Algorithm #Diagnosis #Management #UrinaryTractInfection
Emergency Medicine Cases ... #Pediatric #UTI ... #Algorithm #Diagnosis ... #Management #UrinaryTractInfection ... #Peds
Asymmetrical Tonic Neck Reflex (ATNR)

This primitive reflex found in newborn babies that normally vanishes around 4
position of the infant's ... #Neck #Reflex #PhysicalExam ... #clinical #video ... #Neurology #Peds ... #Pediatrics #Normal
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 ... non-arousable, decr urine ... endocrinology #peds ... #pediatrics