27 results
Preterm Infant Complications - Differential Diagnosis
Respiratory:
 • Transient Tachypnea of the Newborn (TTN)
 • Respiratory Distress
- Differential Diagnosis ... Tachypnea of the Newborn ... Enterocolitis (NEC ... #Causes #Peds # ... Pediatrics
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... The infant's arm ... #clinical #video ... hypotonia #hypotonic #peds ... #pediatrics #tone
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Newborn) - Differential ... Diagnosis Algorithm ... #Peds #Pediatrics
Asymmetrical Tonic Neck Reflex (ATNR)

This primitive reflex found in newborn babies that normally vanishes around 4
reflex found in newborn ... position of the infant's ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
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 ... #Meningitis #Clinical ... #Video #PhysicalExam ... #Pediatrics #Peds
Epiglottitis - Swollen inflamed epiglottis 
Clinical (Rapid onset) 
 • Fever 
 • Sore throat
inflamed epiglottis Clinical ... #Epiglottitis #Signs ... #Causes #Diagnosis ... #Differential #Peds ... #Pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant
Paradoxical Breathing on Physical Exam

Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... It causes the chest ... #respiratory #clinical ... #video #pulmonary ... #peds #pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Passive neck flexion ... causes spinal cord ... Video by Dr. ... #Meningitis #Clinical ... #Pediatrics #Peds
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 ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics