16 results
physicalexam diagnosis reflex management neurology newborn primitive endocrinology normal treatment 21hydroxylasedeficiency 21ohd acromegaly assessment bacterial biliousemesis breathing brudzinskis cardiology cardiomyopathy
Web chart of etiologies related to inflammatory head and neck masses. #pediatrics #peds #differential #causes #pearls #head
#pediatrics #peds ... #differential # ... causes #pearls # ... head #neck #masses ... viral #bacterial #clinical
Epiglottitis - Swollen inflamed epiglottis Clinical (Rapid onset) • Fever • Sore throat
inflamed epiglottis Clinical ... Epiglottitis #Signs #Causes ... #Diagnosis #Differential ... #Peds #Pediatrics
Paradoxical Breathing on Physical Exam Paradoxical breathing is often a sign of breathing problems. It causes the
It causes the chest ... #respiratory #clinical ... #video #pulmonary ... #peds #pediatrics
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 Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
URT inflammation causes ... severe swelling causes ... Meningococcal Toxin C ... #Immunization #peds ... #pediatrics #pathophysiology
How can we break down the differential diagnosis of bilious emesis in infants by age? Image Source:
break down the differential ... : De Virgilio, C. ... Surgery: A case ... based clinical review ... generalsurgery; #pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
tachypnea or wheeze - Clinical ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant ... Tachypnea #Wheeze #Differential
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... Video by Dr. ... Sign #Meningitis #Clinical ... #Pediatrics #Peds
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 Moro Reflex on Newborn Physical Exam The Moro reflex is obtained by holding the baby’s head and
finger forming a “C” ... #Moro #Reflex #Peds ... #Pediatrics #Clinical ... #Video #Neurology
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Galant Reflex on Physical Exam The Galant reflex is present at birth and remains until the 2nd
persistent in cases ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
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