23 results
Aortic Stenosis & Bicuspid Aortic Valve (AS)
 • Introduction & Pathophysiology
 • Classifications
 • Epidemiology
 •
Aortic Valve (AS ... Introduction & Pathophysiology ... Epidemiology • Clinical ... AorticValve #cardiology #peds
Paradoxic Breathing in Pediatric Respiratory Distress - Improved after nebulizers and HFNC

Inward chest wall movement with
with expiration as ... Paradoxical #Pediatrics #Peds ... #clinical #Video
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
In this video, the ... infant cries as ... Sign #Meningitis #Clinical ... #Video #PhysicalExam ... #Pediatrics #Peds
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
While the pathophysiology ... flexion occurs as ... Video by Dr. ... Sign #Meningitis #Clinical ... #Pediatrics #Peds
Difficult Airway Algorithm

1. Assess the likelihood and clinical impact of basic management problems: 
 • Difficulty
Assess the likelihood ... and clinical impact ... intubation • Video-assisted ... laryngoscopy as
Nuchal Rigidity in Infantile Bacterial Meningitis

Flexion of the neck revealed nuchal rigidity. The patient was unable
back from the bed as ... #PhysicalExam #Clinical ... #Video #Peds #Pediatrics
Asymmetrical Tonic Neck Reflex (ATNR)

This primitive reflex found in newborn babies that normally vanishes around 4
Also known as the ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
Nuchal Rigidity in Infantile Bacterial Meningitis

Flexion of the neck revealed nuchal rigidity. The patient was unable
back from the bed as ... #PhysicalExam #Clinical ... #Video #Peds #Pediatrics
Amyotrophic Lateral Sclerosis (ALS) Summary
ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... lateral sclerosis Pathophysiology ... cellular function Clinical ... signs to determine likelihood ... Exam: clinical evidence
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... occur in utero as ... • This is also ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds