3 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... 21-OHase causes varying ... pathophysiology #genetics ... #endocrinology ... #peds #pediatrics
Management of Convulsive Status Epilepticus in children
Stabilization Phase (Seizure 0-5 minutes):
 • Check and maintain ABC
Management of Convulsive ... Check and maintain ABC ... Epilepticus #seizure #Management ... neurology #pediatrics #peds ... #algorithm
Continuous Positive Airway Pressure in the Neonate

WHY CPAP? 
• Maintain airway patency 
• Helps avoid alveoli
baby ABCDE - CARING ... CPAP #Neonate #Management ... #ABCs #ABCDE #Peds