Pediatric Assessment physicalexam algorithm sign brudzinskis peds findings genetics cardiology signs

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12 results

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

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Pediatric Cardiovascular Exam - Infographic Checklist

#PhysicalExam #Cardiovascular #Checklist #Cardiology #Signs #Findings #Peds #Pediatrics #Paediatrics

Pediatric Cardiovascular ... Infographic Checklist #PhysicalExam ... Cardiovascular #Checklist #Cardiology ... #Signs #Findings ... #Peds #Pediatrics

Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized

Brudzinski’s Sign ... sign is characterized ... the sign is not ... Clinical #Video #PhysicalExam ... #Pediatrics #Peds

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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

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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

#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

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