39 results
Brudzinski's Sign on Physical Exam - Meningitis

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... #Brudzinskis #Sign ... #PhysicalExam #clinical ... #video #neurology ... #peds #pediatrics
Bronchiolitis Management

When to admit: 
- Any history of apnoea 
- Persistant sats < 92% 
- Inadequate
Bronchiolitis Management ... fluid intake (<50% normal ... ) Signs of severe ... #diagnosis #Peds ... #Pediatrics #Admission
Epiglottitis - Swollen inflamed epiglottis 
Clinical (Rapid onset) 
 • Fever 
 • Sore throat
inflamed epiglottis Clinical ... #Epiglottitis #Signs ... Causes #Diagnosis #Differential ... #Peds #Pediatrics
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
Kernig's Sign in ... Meningitis Kernig's sign ... #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds #neurology
Cor triatriatum
 • Epidemiology
 • Etiology
 • Associated Lesions
 • Differentials Diagnosis
 • Anatomy - Sinister,
Associated Lesions • Differentials ... Physiology • Clinical ... Post-Operative Management ... cardiology #summary #peds ... #pediatrics
The asphyxia escape reflex is assessed by placing the child in the prone position on the
#PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics ... #Normal #Primitive
Asymmetrical Tonic Neck Reflex (ATNR)

This primitive reflex found in newborn babies that normally vanishes around 4
newborn babies that normally ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics ... #Normal #Primitive
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone ... #normal
American College of Critical Care Medicine algorithm for time-sensitive, goal-directed stepwise management of hemodynamic support in
American College of Critical ... refill ≤ 2s, and normal ... #CriticalCare #Peds ... #Pediatrics #Sepsis ... #Management #StepWise
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... : • Hyperkalemia ... endocrinology #peds ... #pediatrics