The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21ohd anaphylaxis genetics pediatrics treatments
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Anaphylaxis: Treatments (Acute) Additional Info: • IV steroids may be considered for prevention of late phase reactions.
Anaphylaxis: Treatments (Acute ... Anaphylaxis #Treatments #Management ... #pathophysiology ... #immunology
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