23 results
Causes of Depressed / Lethargic Newborn - Differential Diagnosis Algorithm
Maternal Related:
 • Drugs (Ex. SSRI)
 •
- Differential ... Diagnosis Algorithm ... #Differential # ... #Causes #Peds # ... Pediatrics
Preterm Infant Complications - Differential Diagnosis
Respiratory:
 • Transient Tachypnea of the Newborn (TTN)
 • Respiratory Distress
Preterm Infant Complications ... - Differential ... Diagnosis Respiratory ... Tachypnea of the Newborn ... #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
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
shortly after birth ... The skin in this infant ... #clinical #photo ... #peds #pediatrics ... #newborn #perioral
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
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
(Floppy Newborn ... ) - Differential ... Diagnosis Algorithm ... #Causes #Peds # ... Pediatrics
...this infant is large for gestational age (LGA) with a birth weight of about 9 1/2
age (LGA) with a birth ... more glycogen at birth ... #clinical #newborn ... #LGA #large #peds ... #pediatrics
Positive Babinski Reflex with dorsiflexion of the big toe after stroking the sole of the foot.
This
is normal and infants ... flexor response by 12 ... Upgoing #Positive #Peds ... #Pediatrics #Clinical ... #Video #PhysicalExam
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... Other causes #Diagnosis ... #Peds #Pediatrics ... #Wheeze #Differential
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics