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21hydroxylasedeficiency cardiology criticalcare differential endocrinology foamed genetics heartfailure icu management pathophysiology pharmacology table treatment
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
The assessment of ... Signs of congestion ... the determined cause ... #algorithm #management ... #heartfailure #chf
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