15 results
physicalexam clinical newborn meningitis primitive reflex symptoms tone 21hydroxylasedeficiency 21ohd abuse algorithm anomalous apgar babinski brudzinskis cardiology cries disease endocrinology
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
Febrile Child - some diagnostic ... Fever #Evaluation #Assessment ... #Signs #Symptoms ... #PhysicalExam #Diagnosis ... #Peds #Pediatrics
Scarf Sign (Normal) on Physical Exam The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... Exam The scarf sign ... #Scarf #Sign #PhysicalExam ... #clinical #video ... #pediatrics #tone
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 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 ... infant cries as ... Prakash #Kernigs #Sign ... #Peds #neurology
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 Newborn Assessment - APGAR Score Assessment of newborn vital signs following labor via a 10-point scale evaluated
Newborn Assessment ... APGAR Score Assessment ... newborn vital signs ... #Diagnosis #Peds ... #Pediatrics #APGAR
Standardized Physical Abuse Guideline <6 months of age • Social work consult • Skeletal survey • Head
• Troponin for infants ... AST or ALT> 80, signs ... Guidelines #Workup #Peds ... #Pediatrics #Diagnosis
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Brudzinski's sign ... While the pathophysiology ... #PhysicalExam #Pediatrics ... #Peds
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 Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... PVO Present • Diagnosis ... Classic “snowman sign ... management #cardiology #peds ... #pediatrics #summary
CRIES is a 10-point scale, using a physiologic basis similar to APGAR: Crying; Requires increased oxygen
Increased vital signs ... #Diagnosis #Peds ... #Pediatrics #PainScale ... PostOperative #Assessment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
#OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
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