11 results
Pediatric Cardiovascular Exam - Infographic Checklist

#PhysicalExam #Cardiovascular #Checklist #Cardiology #Signs #Findings #Peds #Pediatrics #Paediatrics
Pediatric Cardiovascular ... Infographic Checklist #PhysicalExam ... #Signs #Findings ... #Peds #Pediatrics ... #Paediatrics
Brudzinski's Sign on Physical Exam - Meningitis

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... Meningitis #Brudzinskis ... #Sign #PhysicalExam ... video #neurology #peds ... #pediatrics #meningitis
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Brudzinski’s Sign ... Josef Brudzinski ... ) Brudzinski's ... Clinical #Video #PhysicalExam ... #Pediatrics #Peds
Brudzinski's Sign on Physical Exam - Meningitis

via  @TheIntern254

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics
Brudzinski's Sign ... TheIntern254 #Brudzinskis ... #Sign #PhysicalExam ... video #neurology #peds ... #pediatrics #meningitis
The Febrile Child - some diagnostic clues to evaluating the febrile child.

#Febrile #Fever #Evaluation #Assessment #Signs
Fever #Evaluation #Assessment ... #Signs #Symptoms ... #PhysicalExam # ... Diagnosis #Peds ... #Pediatrics
Rapid Assessment of the Neonate With Sonography (RANS) Scan

Recommended algorithm for RANS scan. 
* Abnormal vital
Rapid Assessment ... Recommended algorithm ... Abnormal vital signs ... Sonography #Neonate #Peds ... #Pediatrics #Neonatology
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical findings ... Prader-Willi Syndrome Signs ... PraderWilli #Syndrome #genetics ... pathophysiology #peds ... #pediatrics
Clinical features of Liver Disease in Children

#Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology

**
#LiverFailure #Signs ... #Symptoms #PhysicalExam ... #Findings #Diagnosis ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical Findings ... Signs/Symptoms/Complications ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
Check for classic findings ... purposes of this algorithm ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki