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pediatrics 21hydroxylasedeficiency 21ohd abcde abcs neonate pathophysiology
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
Continuous Positive Airway Pressure in the Neonate WHY CPAP? • Maintain airway patency • Helps avoid alveoli
Neonate WHY CPAP ... baby ABCDE - CARING ... FOR A BABY ON CPAP ... #Neonate #Management ... #ABCs #ABCDE #Peds
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