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21hydroxylasedeficiency 21ohd combination inhalers labaics names naming pathophysiology pediatrics peds pharmacology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... wasting crisis & hyperkalemia ... Complications: • Hyperkalemia ... pathophysiology #genetics ... #endocrinology
LABA/ICS Combination Inhalers Long-Acting Beta2 Agonists (LABA) + Inhaled Corticosteroid (ICS) - Commonly used in Asthma Advair
Commonly used in Asthma ... commonly used in asthma ... COPD treatment algorithm ... are the normal dosing ... available in a generic
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